Canonical Allele Identifier: PA915956947
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 381716
ClinVar RCV Id: RCV000425954 RCV000504529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Gly650Arg
CA2660874
NM_000096.4:c.1948G>A
CA354932541
NM_000096.4:c.1948G>C