Canonical Allele Identifier: PA150395
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 98307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Thr395Met
CA150394
NM_000744.7:c.1184C>T