Canonical Allele Identifier: PA1139678771
Gene: CHRNA4 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.Ser284Trp
CA409636492
NM_000744.7:c.851C>G