Canonical Allele Identifier: PA2828806899
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2047132
ClinVar RCV Id: RCV002904071 RCV004066201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Leu539Gln
CA4991185
NM_001379081.2:c.1616T>A