Canonical Allele Identifier: PA2825638883
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2746817
ClinVar RCV Id: RCV003536583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Tyr719Phe
CA16026174
NM_001127511.3:c.2156A>T