Canonical Allele Identifier: PA2828044016
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly1795Ser
CA16033936
NM_001354904.2:c.5383G>A