Canonical Allele Identifier: PA150381
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 98300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Ser334Leu
CA150380
NM_000744.7:c.1001C>T