Canonical Allele Identifier: PA2827993646
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gly913Ser
CA033918
NM_001354901.2:c.2737G>A