Allele Registry

Canonical Allele Identifier: PA658808733

Gene: HSPB8 HGNC NCBI

ClinVar Variation Id: 533139

HGVS (amino-acid)	Matching Registered Transcripts
NP_055180.1:p.Ala168Val	CA6819618 NM_014365.3:c.503C>T