Canonical Allele Identifier: PA127372
Gene: BSG HGNC NCBI

Linked Data

ClinVar Variation Id: 17751
ClinVar RCV Id: RCV000019327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940991.1:p.Glu92Lys
CA127371
NM_198589.3:c.274G>A