Canonical Allele Identifier: PA891858127
Gene: NEXMIF HGNC NCBI

Linked Data

ClinVar Variation Id: 573146
ClinVar RCV Id: RCV001307364
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008537.1:p.Ser1192Pro
CA413665386
NM_001008537.3:c.3574T>C