Canonical Allele Identifier: PA2827987250
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1697525
ClinVar RCV Id: RCV002268809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1738Leu
CA16032993
NM_001354900.2:c.5212A>C
CA16032995
NM_001354900.2:c.5212A>T