Canonical Allele Identifier: PA130189
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 37203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Asp211Val
CA033058
NM_000402.4:c.[632A>T;466A>G]
CA130188
NM_000402.4:c.632A>T