Canonical Allele Identifier: PA2827993868
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg981Trp
CA008046
NM_001354901.2:c.2941A>T