Canonical Allele Identifier: PA2742033253
Gene: HSPD1 HGNC NCBI
ClinVar RCV:
RCV003750432
ClinVar Variation:
2882695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955472.1:p.Ser252Ala
CA2043508
NM_199440.2:c.754T>G