Canonical Allele Identifier: PA2829360217
Gene: HSPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2057380
ClinVar RCV Id: RCV002914845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002147.2:p.Gln377Arg
CA350199459
NM_002156.5:c.1130A>G