Canonical Allele Identifier: PA658800084
Gene: NEXMIF HGNC NCBI

Linked Data

ClinVar Variation Id: 541119
ClinVar RCV Id: RCV000651323 RCV002485471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001008537.1:p.Ser747Arg
CA10455064
NM_001008537.3:c.2241C>A
CA413668655
NM_001008537.3:c.2241C>G
CA413668661
NM_001008537.3:c.2239A>C