Canonical Allele Identifier: PA916018210
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 531901
ClinVar RCV Id: RCV000638458 RCV002438693
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278796.1:p.Thr970Met
CA10358774
NM_001291867.2:c.2909C>T