Canonical Allele Identifier: PA103432
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 11426
ClinVar RCV Id: RCV000012179 RCV002512978
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123237.1:p.Ala105Val
CA341090
NM_001129765.2:c.314C>T