Canonical Allele Identifier: PA915989313
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 21265
ClinVar RCV Id: RCV000020427 RCV002514124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Tyr349Cys
CA341814
NM_015922.2:c.1046A>G