Canonical Allele Identifier: PA2828057978
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 10383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001346945.1:p.Val213Leu
CA120984
NM_001360016.2:c.637G>T
CA10566205
NM_001360016.2:c.637G>C