Canonical Allele Identifier: PA915986323
Gene: HSF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7095
ClinVar RCV Id: RCV000007512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001529.2:p.Ile86Val
CA118627
NM_001538.4:c.256A>G