Canonical Allele Identifier: PA118830
Gene: HSPB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 7483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001531.1:p.Pro182Ser
CA118828
NM_001540.5:c.544C>T