Allele Registry

Canonical Allele Identifier: PA645502357

Gene: FREM2 HGNC NCBI

ClinVar Variation Id: 311950

HGVS (amino-acid)	Matching Registered Transcripts
NP_997244.4:p.Phe549Leu	CA6954455 NM_207361.6:c.1647C>A CA387886575 NM_207361.6:c.1645T>C CA387886587 NM_207361.6:c.1647C>G