Canonical Allele Identifier: PA645440855
Gene: CHRNG HGNC NCBI

Linked Data

ClinVar Variation Id: 259667
ClinVar RCV Id: RCV000249476 RCV000271778 RCV000342579 RCV001094660 RCV001640534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005190.4:p.Ala149Thr
CA2168670
NM_005199.5:c.445G>A