Canonical Allele Identifier: PA2825838030
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 16197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135741.1:p.Arg428Pro
CA126264
NM_001142269.2:c.1283G>C