Canonical Allele Identifier: PA2580105754
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 1700496
ClinVar RCV Id: RCV002274745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Pro450Leu
CA287217471
NM_000173.7:c.1349C>T