Canonical Allele Identifier: PA2827995882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949271
ClinVar RCV Id: RCV003650743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1591Tyr
CA16032166
NM_001354901.2:c.4771A>T