Canonical Allele Identifier: PA913198397
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 634555
ClinVar RCV Id: RCV000785066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Thr166Ser
CA409638345
NM_000744.7:c.497C>G
CA409638350
NM_000744.7:c.496A>T