Canonical Allele Identifier: PA103450
Gene: NSDHL HGNC NCBI
ClinVar Allele:
26466
ClinVar RCV:
RCV000012180
ClinVar Variation:
11427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123237.1:p.Gly205Ser
CA341091
NM_001129765.2:c.613G>A