Canonical Allele Identifier: PA2829360276
Gene: HSPE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3107399
ClinVar RCV Id: RCV004404753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002148.1:p.Asp93Val
CA350205902
NM_002157.3:c.278A>T