Canonical Allele Identifier: PA2827953365
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3074632
ClinVar RCV Id: RCV004014166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2626Val
CA16038328
NM_001354896.2:c.7877C>T