Canonical Allele Identifier: PA2828007722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573474
ClinVar RCV Id: RCV003534634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1580Thr
CA16032737
NM_001354905.2:c.4738C>A