Canonical Allele Identifier: PA645502440
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 283801
ClinVar RCV Id: RCV000280744 RCV000725336 RCV003930086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Thr3013Met
CA6956299
NM_207361.6:c.9038C>T