Canonical Allele Identifier: PA2828029320
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3074632
ClinVar RCV Id: RCV004014166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala2507Val
CA16038328
NM_001354903.2:c.7520C>T