Canonical Allele Identifier: PA2827962049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1351612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2459Gly
CA16037326
NM_001354897.2:c.7375A>G