Canonical Allele Identifier: PA2825021586
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser1757Tyr
CA16032851
NM_000038.6:c.5270C>A