Canonical Allele Identifier: PA2828002385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 940870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1440Ser
CA16031388
NM_001354902.2:c.4319A>G