Canonical Allele Identifier: PA2573223463
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406612
ClinVar RCV Id: RCV001935483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Val251Leu
CA352230059
NM_001904.4:c.751G>C
CA352230061
NM_001904.4:c.751G>T