Canonical Allele Identifier: PA645502423
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 284704
ClinVar RCV Id: RCV000348468 RCV000767220 RCV000767221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Arg2167Trp
CA6955578
NM_207361.6:c.6499C>T