Canonical Allele Identifier: PA107449
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 11929
ClinVar RCV Id: RCV000012705 RCV000221789 RCV000191108 RCV000627780 RCV000791161 RCV000999977 RCV001270083 RCV002262563 RCV002512987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Val377Ile
CA121776
NM_000431.4:c.1129G>A