Canonical Allele Identifier: PA2829340117
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_001719.2:p.Glu208Lys
CA127371
NM_001728.4:c.622G>A