Canonical Allele Identifier: PA2827879740
Gene: IVD HGNC NCBI

Linked Data

ClinVar Variation Id: 2228292
ClinVar RCV Id: RCV002707573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341526.1:p.Asn152Lys
CA391717137
NM_001354597.3:c.456T>A
CA391717138
NM_001354597.3:c.456T>G