Canonical Allele Identifier: PA2828011859
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2334Asn
CA16037169
NM_001354902.2:c.7001G>A