Canonical Allele Identifier: PA2825638105
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala431Val
CA16024253
NM_001127511.3:c.1292C>T