Canonical Allele Identifier: PA313459
Gene: CHRNA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 204968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000733.2:p.Ser358Ile
CA313458
NM_000742.4:c.1073G>T