Allele Registry

Canonical Allele Identifier: PA094687

Gene: HSPB8 HGNC NCBI

ClinVar RCV:

RCV000002736

RCV001216811

RCV001532719

ClinVar Variation:

2618

HGVS (amino-acid)	Matching Registered Transcripts
NP_055180.1:p.Lys141Glu	CA115644 NM_014365.3:c.421A>G