Canonical Allele Identifier: PA1139687705
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 843687
ClinVar RCV Id: RCV001046363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Asp38His
CA322079798
NM_000407.5:c.112G>C