Canonical Allele Identifier: PA2827880980
Gene: IVD HGNC NCBI

Linked Data

ClinVar Variation Id: 3112020
ClinVar RCV Id: RCV004400948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341530.2:p.Trp81Ser
CA7480566
NM_001354601.3:c.242G>C