Canonical Allele Identifier: PA916037999
Gene: IVD HGNC NCBI
ClinVar Allele:
200289
ClinVar RCV:
RCV000412245
ClinVar Variation:
203792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341529.2:p.Ala326Val
CA312669
NM_001354600.3:c.977C>T