Canonical Allele Identifier: PA2573163914
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 1679420
ClinVar RCV Id: RCV002227300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.His219Gln
CA397317914
NM_000173.7:c.657C>A
CA397317916
NM_000173.7:c.657C>G