Canonical Allele Identifier: PA645491409
Gene: FRG2B HGNC NCBI

Linked Data

ClinVar Variation Id: 402881
ClinVar RCV Id: RCV000454963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001074467.1:p.His11Tyr
CA5768715
NM_001080998.2:c.31C>T