Canonical Allele Identifier: PA2827956073
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg633Trp
CA006202
NM_001354897.2:c.1897C>T