Canonical Allele Identifier: PA2825633591
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1757Tyr
CA16032851
NM_001127510.3:c.5270C>A