Canonical Allele Identifier: PA2826219727
Gene: GCLC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184044.1:p.Ile543Met
CA3859960
NM_001197115.2:c.1629C>G