Canonical Allele Identifier: PA2828004580
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2694His
CA050563
NM_001354902.2:c.8080A>C