Canonical Allele Identifier: PA645440933
Gene: CHRNG HGNC NCBI

Linked Data

ClinVar Variation Id: 235269
ClinVar RCV Id: RCV000224861 RCV000509333 RCV001141631 RCV001141632 RCV004541362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005190.4:p.Ser372Phe
CA2168943
NM_005199.5:c.1115C>T