Canonical Allele Identifier: PA916042432
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 646667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn992Thr
CA035129
NM_001354904.2:c.2975A>C