Canonical Allele Identifier: PA916042318
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala15Val
CA16021438
NM_001354903.2:c.44C>T