Allele Registry

Canonical Allele Identifier: PA094672

Gene: HSPB8 HGNC NCBI

ClinVar RCV:

RCV000002735

RCV000002737

RCV000192250

RCV002472922

ClinVar Variation:

2617

2619

HGVS (amino-acid)	Matching Registered Transcripts
NP_055180.1:p.Lys141Asn	CA115642 NM_014365.3:c.423G>C CA252366 NM_014365.3:c.423G>T