Canonical Allele Identifier: PA2828002692
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1058153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly1583Glu
CA16032317
NM_001354902.2:c.4748G>A