Canonical Allele Identifier: PA2827980763
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 921617
ClinVar RCV Id: RCV001181165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2544Leu
CA16038090
NM_001354899.2:c.7631C>T