Canonical Allele Identifier: PA915956916
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 343779
ClinVar RCV Id: RCV000326860 RCV002520098 RCV003480611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Thr313Ile
CA2661194
NM_000096.4:c.938C>T