Canonical Allele Identifier: PA916042514
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Tyr983Cys
CA16028846
NM_001354905.2:c.2948A>G