Canonical Allele Identifier: PA2828018981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1315725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asp915Tyr
CA16028002
NM_001354903.2:c.2743G>T