Allele Registry

Canonical Allele Identifier: PA207669

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000193889

RCV003621519

ClinVar Variation:

211595

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