Allele Registry

Canonical Allele Identifier: PA101971

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV000000955

RCV003328549

RCV003398406

ClinVar Variation:

907

HGVS (amino-acid)	Matching Registered Transcripts
NP_000172.2:p.Trp627Cys	CA339854 NM_000181.4:c.1881G>T CA367637241 NM_000181.4:c.1881G>C