Allele Registry

Canonical Allele Identifier: PA3057318410

Gene: GGCX HGNC NCBI

ClinVar RCV:

RCV004722320

ClinVar Variation:

3341038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135741.1:p.Arg428His	CA1741804 NM_001142269.2:c.1283G>A