Canonical Allele Identifier: PA2829360185
Gene: HSPD1 HGNC NCBI
ClinVar RCV:
RCV003750432
ClinVar Variation:
2882695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002147.2:p.Ser252Ala
CA2043508
NM_002156.5:c.754T>G