Canonical Allele Identifier: PA2828807140
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049575
ClinVar RCV Id: RCV001355868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Leu1402Val
CA372966391
NM_001379081.2:c.4204C>G