Canonical Allele Identifier: PA2580252086
Gene: GCLC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001489.1:p.Arg427Pro
CA364470663
NM_001498.4:c.1280G>C