Canonical Allele Identifier: PA645491410
Gene: FRG2B HGNC NCBI

Linked Data

ClinVar Variation Id: 402880
ClinVar RCV Id: RCV000456047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001074467.1:p.His11Gln
CA5768713
NM_001080998.2:c.33C>G
CA378842551
NM_001080998.2:c.33C>A