Canonical Allele Identifier: PA2580105734
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 1693270
ClinVar RCV Id: RCV002260538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Leu194Phe
CA8314801
NM_000173.7:c.580C>T