Canonical Allele Identifier: PA343922
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 41029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Arg336His
CA343921
NM_000744.7:c.1007G>A