Canonical Allele Identifier: PA915956935
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 210755
ClinVar RCV Id: RCV000192950 RCV000398768 RCV001355940 RCV003917744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Pro477Leu
CA206118
NM_000096.4:c.1430C>T