Canonical Allele Identifier: PA2580111148
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 2085325
ClinVar RCV Id: RCV003005006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Thr536Ser
CA10565979
NM_000402.4:c.1607C>G
CA415231879
NM_000402.4:c.1606A>T