Canonical Allele Identifier: PA915956875
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 521552
ClinVar RCV Id: RCV000624072 RCV000809524 RCV001584450 RCV003117432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Gly195Arg
CA2661289
NM_000096.4:c.583G>A
CA354917198
NM_000096.4:c.583G>C