Canonical Allele Identifier: PA2826400077
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 205017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243502.1:p.Ala335Ser
CA313551
NM_001256573.2:c.1003G>T