Canonical Allele Identifier: PA272344
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 159453
ClinVar RCV Id: RCV000146964 RCV000412977
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Val243Met
CA272342
NM_015922.2:c.727G>A