Canonical Allele Identifier: PA2828009667
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 952914
ClinVar RCV Id: RCV003650776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser1665Pro
CA16032844
NM_001354902.2:c.4993T>C