Canonical Allele Identifier: PA645426642
Gene: GP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 257422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057447.5:p.Pro219Ser
CA310128585
NM_016363.5:c.655C>T