Canonical Allele Identifier: PA2573169421
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 1691254
ClinVar RCV Id: RCV002254240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Pro90Ser
CA410676953
NM_000407.5:c.268C>T