Allele Registry

Canonical Allele Identifier: PA103123

Gene: HSPD1 HGNC NCBI

ClinVar RCV:

RCV000019112

ClinVar Variation:

17557

HGVS (amino-acid)	Matching Registered Transcripts
NP_002147.2:p.Val98Ile	CA127251 NM_002156.5:c.292G>A