Canonical Allele Identifier: PA2828018826
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala722Val
CA10578347
NM_001354906.2:c.2165C>T