Canonical Allele Identifier: PA645440857
Gene: CHRNG HGNC NCBI

Linked Data

ClinVar Variation Id: 335003
ClinVar RCV Id: RCV000275954 RCV001094713 RCV002521417
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005190.4:p.Val154Ile
CA2168672
NM_005199.5:c.460G>A