Canonical Allele Identifier: PA2828058260
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 2085325
ClinVar RCV Id: RCV003005006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001346945.1:p.Thr506Ser
CA10565979
NM_001360016.2:c.1517C>G
CA415231879
NM_001360016.2:c.1516A>T