Allele Registry

Canonical Allele Identifier: PA121786

Gene: MVK HGNC NCBI

ClinVar RCV:

RCV000012711

RCV001219913

ClinVar Variation:

11933

HGVS (amino-acid)	Matching Registered Transcripts
NP_000422.1:p.Pro165Leu	CA121784 NM_000431.4:c.494C>T