Canonical Allele Identifier: PA2828007494
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745359
ClinVar RCV Id: RCV002336002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln1541Pro
CA16032485
NM_001354905.2:c.4622A>C