Canonical Allele Identifier: PA658669987
Gene: ME2 HGNC NCBI

Linked Data

ClinVar Variation Id: 447713
ClinVar RCV Id: RCV000516806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002387.1:p.Ile137Val
CA8965058
NM_002396.5:c.409A>G