Canonical Allele Identifier: PA1139742780
Gene: FREM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 976625
ClinVar RCV Id: RCV001253981 RCV002485993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356989.1:p.Asp317His
CA4991410
NM_001370060.1:c.949G>C