Canonical Allele Identifier: PA2580570118
Gene: HSPD1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955472.1:p.Gln377Arg
CA350199459
NM_199440.2:c.1130A>G