Canonical Allele Identifier: PA915989269
Gene: NSDHL HGNC NCBI
ClinVar RCV:
RCV000012183
ClinVar Variation:
11430
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057006.1:p.Ala182Pro
CA255884
NM_015922.2:c.544G>C