Allele Registry

Canonical Allele Identifier: PA111042

Gene: GGCX HGNC NCBI

ClinVar RCV:

RCV000017581

RCV003556035

ClinVar Variation:

16197

HGVS (amino-acid)	Matching Registered Transcripts
NP_000812.2:p.Arg485Pro	CA126264 NM_000821.7:c.1454G>C