Canonical Allele Identifier: PA1139682218
Gene: GGCX HGNC NCBI

Linked Data

ClinVar Variation Id: 895043
ClinVar RCV Id: RCV001136911
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Arg485Cys
CA1741805
NM_000821.7:c.1453C>T