Canonical Allele Identifier: PA2828048517
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala2458Ser
CA16038165
NM_001354904.2:c.7372G>T