Canonical Allele Identifier: PA2828046997
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 852832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2251His
CA16036858
NM_001354904.2:c.6751A>C