Canonical Allele Identifier: PA127252
Gene: HSPD1 HGNC NCBI
ClinVar RCV:
RCV000019112
ClinVar Variation:
17557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955472.1:p.Val98Ile
CA127251
NM_199440.2:c.292G>A