Canonical Allele Identifier: PA297730
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala385Val
CA004066
NM_001127510.3:c.1154C>T