Canonical Allele Identifier: PA2828534078
Gene: HSF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 459608
ClinVar RCV Id: RCV000531113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361603.1:p.Val117Gly
CA396264554
NM_001374674.1:c.350T>G