Canonical Allele Identifier: PA2827992859
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2746817
ClinVar RCV Id: RCV003536583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Tyr678Phe
CA16026174
NM_001354901.2:c.2033A>T