Allele Registry

Canonical Allele Identifier: PA916018184

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000193889

RCV003621519

ClinVar Variation:

211595

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Ser388Leu	CA207668 NM_001291867.2:c.1163C>T