Canonical Allele Identifier: PA1139730930
Gene: CHRNG HGNC NCBI

Linked Data

ClinVar Variation Id: 896328
ClinVar RCV Id: RCV001138916 RCV001138915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005190.4:p.Arg147Leu
CA351009003
NM_005199.5:c.440G>T