Canonical Allele Identifier: PA2826143041
Gene: GPI HGNC NCBI

Linked Data

ClinVar Variation Id: 1175178
ClinVar RCV Id: RCV001530174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171651.1:p.His549Gln
CA9367493
NM_001184722.1:c.1647C>G
CA307634822
NM_001184722.1:c.1647C>A