Canonical Allele Identifier: PA2827992745
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala638Val
CA030702
NM_001354901.2:c.1913C>T