Canonical Allele Identifier: PA2827984726
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 844658
ClinVar RCV Id: RCV003649314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly978Val
CA16028028
NM_001354900.2:c.2933G>T