Canonical Allele Identifier: PA645502435
Gene: FREM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 312031
ClinVar RCV Id: RCV000268713 RCV001356115 RCV003950060 RCV002487382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_997244.4:p.Pro2837Ser
CA6956151
NM_207361.6:c.8509C>T