Canonical Allele Identifier: PA2828023518
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1059798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln1469Glu
CA16032822
NM_001354906.2:c.4405C>G