Canonical Allele Identifier: PA645493473
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 375706
ClinVar RCV Id: RCV000498961
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_938011.1:p.Ser1462Cys
CA412370422
NM_198270.4:c.4385C>G