Canonical Allele Identifier: PA2828003915
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 852832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2286His
CA16036858
NM_001354902.2:c.6856A>C