Canonical Allele Identifier: PA915989271
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 11427
ClinVar RCV Id: RCV000012180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Gly205Ser
CA341091
NM_015922.2:c.613G>A