Canonical Allele Identifier: PA658800080
Gene: NEXMIF HGNC NCBI

Linked Data

ClinVar Variation Id: 541127
ClinVar RCV Id: RCV000651331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008537.1:p.Thr597Ala
CA331301777
NM_001008537.3:c.1789A>G