Canonical Allele Identifier: PA916042418
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala981Ser
CA16028614
NM_001354904.2:c.2941G>T