Canonical Allele Identifier: PA203354
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 198289
ClinVar RCV Id: RCV000179566 RCV000876610 RCV002317057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_938011.1:p.Ser1104Leu
CA203353
NM_198270.4:c.3311C>T