Allele Registry

Canonical Allele Identifier: PA2826314840

Gene: HSF2 HGNC NCBI

ClinVar RCV:

RCV004134635

ClinVar Variation:

2285006

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230023.1:p.Lys128Arg	CA365482011 NM_001243094.2:c.383A>G