Canonical Allele Identifier: PA2828004515
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala2639Asp
CA16039108
NM_001354902.2:c.7916C>A