Canonical Allele Identifier: PA2826219709
Gene: GCLC HGNC NCBI

Linked Data

ClinVar Variation Id: 2432086
ClinVar RCV Id: RCV003131004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184044.1:p.Arg389Pro
CA364470663
NM_001197115.2:c.1166G>C