Canonical Allele Identifier: PA2828023213
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 924017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser1423Pro
CA16032513
NM_001354906.2:c.4267T>C