Canonical Allele Identifier: PA2825515613
Gene: GP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2266922
ClinVar RCV Id: RCV002803706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077368.2:p.Ser246Gly
CA407479260
NM_001083899.2:c.736A>G