Canonical Allele Identifier: PA207669
Gene: NHS HGNC NCBI

Linked Data

ClinVar Variation Id: 211595
ClinVar RCV Id: RCV000193889 RCV003621519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_938011.1:p.Ser367Leu
CA207668
NM_198270.4:c.1100C>T