Allele Registry

Canonical Allele Identifier: PA645502356

Gene: FREM2 HGNC NCBI

ClinVar Variation Id: 311949

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Arg535Cys	CA6954442 NM_207361.6:c.1603C>T