Canonical Allele Identifier: PA2828042982
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1697525
ClinVar RCV Id: RCV002268809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1653Leu
CA16032993
NM_001354904.2:c.4957A>C
CA16032995
NM_001354904.2:c.4957A>T