Canonical Allele Identifier: PA2825524752
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 444598
ClinVar RCV Id: RCV000513017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Met14Val
CA2330855
NM_001098209.1:c.40A>G