Canonical Allele Identifier: PA2827942482
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gly972Ser
CA033918
NM_001354895.2:c.2914G>A