Canonical Allele Identifier: PA127280
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17586
ClinVar RCV Id: RCV000019151 RCV000426489 RCV000427490 RCV000420061 RCV000437726 RCV000433883 RCV000442576 RCV000444520 RCV000445320 RCV000425340 RCV000428583 RCV000436738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Ser37Phe
CA127279
NM_001904.4:c.110C>T