Allele Registry

Canonical Allele Identifier: PA170994

Gene: MTR HGNC NCBI

ClinVar RCV:

RCV000015355

RCV000126868

RCV000144923

RCV000398009

RCV001519615

RCV001812069

RCV003982899

ClinVar Variation:

138289

HGVS (amino-acid)	Matching Registered Transcripts
NP_000245.2:p.Asp919Gly	CA170993 NM_000254.3:c.2756A>G