Canonical Allele Identifier: PA2573315497
Gene: HSPD1 HGNC NCBI
ClinVar RCV:
RCV002008395
ClinVar Variation:
1485089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955472.1:p.Met356Arg
CA350199695
NM_199440.2:c.1067T>G