Canonical Allele Identifier: PA2828002387
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1440His
CA16031385
NM_001354902.2:c.4318A>C