Canonical Allele Identifier: PA313542
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 205012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Pro169Arg
CA313541
NM_000744.7:c.506C>G