Canonical Allele Identifier: PA916009516
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 205014
ClinVar RCV Id: RCV000186925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243502.1:p.Trp6Arg
CA313545
NM_001256573.2:c.16T>C
CA409638055
NM_001256573.2:c.16T>A