Allele Registry

Canonical Allele Identifier: PA094687

Gene: HSPB8 HGNC NCBI

ClinVar Variation Id: 2618

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