Canonical Allele Identifier: PA2827998730
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Tyr2458Cys
CA013809
NM_001354901.2:c.7373A>G