Canonical Allele Identifier: PA2827971688
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933245
ClinVar RCV Id: RCV003538603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2576Thr
CA16038278
NM_001354898.2:c.7727G>C