Allele Registry

Canonical Allele Identifier: PA127254

Gene: HSPD1 HGNC NCBI

ClinVar RCV:

RCV000019113

ClinVar Variation:

17558

HGVS (amino-acid)	Matching Registered Transcripts
NP_955472.1:p.Asp29Gly	CA127253 NM_199440.2:c.86A>G