Canonical Allele Identifier: PA2828017350
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser504Gly
CA031761
NM_001354906.2:c.1510A>G