Canonical Allele Identifier: PA313465
Gene: CHRNA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 204971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000733.2:p.Pro383Leu
CA313464
NM_000742.4:c.1148C>T