Allele Registry

Canonical Allele Identifier: PA174929

Gene: CSF2RB HGNC NCBI

ClinVar RCV:

RCV000149403

RCV001850024

ClinVar Variation:

161978

HGVS (amino-acid)	Matching Registered Transcripts
NP_000386.1:p.Ser271Leu	CA174928 NM_000395.3:c.812C>T