Canonical Allele Identifier: PA2741955965
Gene: NSDHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2910363
ClinVar RCV Id: RCV003734647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Asp154Asn
CA415285210
NM_015922.2:c.460G>A