Canonical Allele Identifier: PA103123
Gene: HSPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17557
ClinVar RCV Id: RCV000019112
JSON-LD

Amino-acid Alleles

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