Canonical Allele Identifier: PA2828055650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 646667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn958Thr
CA035129
NM_001354905.2:c.2873A>C