Canonical Allele Identifier: PA2828018930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala904Val
CA10578347
NM_001354903.2:c.2711C>T