Canonical Allele Identifier: PA915989259
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 11426
ClinVar RCV Id: RCV000012179 RCV002512978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Ala105Val
CA341090
NM_015922.2:c.314C>T