Canonical Allele Identifier: PA174651
Gene: BRF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161715
ClinVar RCV Id: RCV000149251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060780.2:p.Ala93Thr
CA174650
NM_018310.4:c.277G>A