Canonical Allele Identifier: PA150385
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 98302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Val352Met
CA150384
NM_000744.7:c.1054G>A