Canonical Allele Identifier: PA645440845
Gene: CHRNG HGNC NCBI

Linked Data

ClinVar Variation Id: 397615
ClinVar RCV Id: RCV000449634 RCV000762330 RCV001007785 RCV003479120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005190.4:p.Arg86Cys
CA2168586
NM_005199.5:c.256C>T