Canonical Allele Identifier: PA2827998863
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 827187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2498Phe
CA16037995
NM_001354901.2:c.7493C>T