Canonical Allele Identifier: PA2827996602
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1812Tyr
CA042401
NM_001354901.2:c.5434G>T