Canonical Allele Identifier: PA915956922
Gene: CP HGNC NCBI
ClinVar RCV:
RCV000584748
ClinVar Variation:
488147
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Cys338Ser
CA2661175
NM_000096.4:c.1012T>A
CA354913833
NM_000096.4:c.1013G>C