Allele Registry

Canonical Allele Identifier: PA645502349

Gene: FREM2 HGNC NCBI

ClinVar Variation Id: 311938

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Gln178Lys	CA6954225 NM_207361.6:c.532C>A