Canonical Allele Identifier: PA916018351
Gene: MTR HGNC NCBI

Linked Data

ClinVar Variation Id: 534572
ClinVar RCV Id: RCV000642168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278868.1:p.Leu356Ser
CA345391867
NM_001291939.1:c.1067T>C