Canonical Allele Identifier: PA2573223471
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368821
ClinVar RCV Id: RCV001867688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Met271_Ala272del
CA2573136981
NM_001904.4:c.811_816del