Allele Registry

Canonical Allele Identifier: PA658667903

Gene: HSPB8 HGNC NCBI

ClinVar RCV:

RCV000538374

RCV003278890

ClinVar Variation:

464509

HGVS (amino-acid)	Matching Registered Transcripts
NP_055180.1:p.Pro89Gln	CA6819539 NM_014365.3:c.266C>A