Allele Registry

Canonical Allele Identifier: PA2826314838

Gene: HSF2 HGNC NCBI

ClinVar RCV:

RCV004120431

ClinVar Variation:

2264171

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230023.1:p.Arg122Gly	CA365481931 NM_001243094.2:c.364C>G