Canonical Allele Identifier: PA099993
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30767
ClinVar RCV Id: RCV000023746 RCV000059636 RCV000207399 RCV000988143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.Arg498Gln
CA129451
NM_144966.7:c.1493G>A