Canonical Allele Identifier: PA2827881067
Gene: IVD HGNC NCBI

Linked Data

ClinVar Variation Id: 2228292
ClinVar RCV Id: RCV002707573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341530.2:p.Asn168Lys
CA391717137
NM_001354601.3:c.504T>A
CA391717138
NM_001354601.3:c.504T>G