Canonical Allele Identifier: PA2825809727
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 375706
ClinVar RCV Id: RCV000498961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129496.1:p.Ser1306Cys
CA412370422
NM_001136024.4:c.3917C>G