Canonical Allele Identifier: PA2828028093
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1006546
ClinVar RCV Id: RCV003770565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2158Thr
CA16037273
NM_001354906.2:c.6472T>A