Canonical Allele Identifier: PA2580138338
Gene: GP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2179397
ClinVar RCV Id: RCV002599034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077368.2:p.Lys323Ser
CA2580097800
NM_001083899.2:c.967_968delinsTC