Canonical Allele Identifier: PA094696
Gene: HSF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7093
ClinVar RCV Id: RCV000007510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035757.1:p.Arg119Cys
CA118625
NM_001040667.3:c.355C>T