Canonical Allele Identifier: PA2826368592
Gene: GP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2266922
ClinVar RCV Id: RCV002803706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242946.2:p.Ser228Gly
CA407479260
NM_001256017.2:c.682A>G