Canonical Allele Identifier: PA2580521008
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1948344
ClinVar RCV Id: RCV002667664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659403.4:p.His1469Tyr
CA372965987
NM_144966.7:c.4405C>T