Canonical Allele Identifier: PA2828036388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala879Val
CA10578347
NM_001354904.2:c.2636C>T