Canonical Allele Identifier: PA100038
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30764
ClinVar RCV Id: RCV000023743 RCV000059638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Leu1324Arg
CA219848
NM_144966.7:c.3971T>G