Canonical Allele Identifier: PA2828002749
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1609Val
CA10578393
NM_001354902.2:c.4826C>T