Canonical Allele Identifier: PA2499234062
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1030886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Trp343Cys
CA409635490
NM_000744.7:c.1029G>T
CA409635493
NM_000744.7:c.1029G>C