Canonical Allele Identifier: PA2828024530
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gly1638Ser
CA16033936
NM_001354906.2:c.4912G>A