Canonical Allele Identifier: PA645502404
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 311991
ClinVar RCV Id: RCV000360002 RCV001701948 RCV003930332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Gly1806Asp
CA6955250
NM_207361.6:c.5417G>A