Canonical Allele Identifier: PA2829360211
Gene: HSPD1 HGNC NCBI
ClinVar RCV:
RCV002008395
ClinVar Variation:
1485089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002147.2:p.Met356Arg
CA350199695
NM_002156.5:c.1067T>G