Canonical Allele Identifier: PA118833
Gene: HSPB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001531.1:p.Arg140Gly
CA118831
NM_001540.5:c.418C>G