Canonical Allele Identifier: PA1139678771
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 969721
ClinVar RCV Id: RCV001245132
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Amino-acid Alleles

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