Canonical Allele Identifier: PA246763
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 159452
ClinVar RCV Id: RCV000146963 RCV000179494
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Arg199Cys
CA246761
NM_015922.2:c.595C>T