Canonical Allele Identifier: PA645495866
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376232
ClinVar RCV Id: RCV000426895 RCV000444074 RCV003332169
ClinVar Variation Id: 376233
ClinVar RCV Id: RCV000418083 RCV000420040 RCV000419419 RCV000427501 RCV000427907 RCV000430713 RCV000436663 RCV000438184 RCV000438776 RCV000438599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Gly34Arg
CA16602685
NM_001904.4:c.100G>A
CA16602686
NM_001904.4:c.100G>C