Canonical Allele Identifier: PA2573223459
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429766
ClinVar RCV Id: RCV001950168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Ala239Ser
CA352229915
NM_001904.4:c.715G>T