Canonical Allele Identifier: PA2828806995
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2150693
ClinVar RCV Id: RCV003067700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366010.1:p.Asp922Asn
CA4990821
NM_001379081.2:c.2764G>A