Canonical Allele Identifier: PA2828017109
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala634Val
CA007259
NM_001354903.2:c.1901C>T