Canonical Allele Identifier: PA150439
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 98329
ClinVar RCV Id: RCV000084619 RCV001064577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000735.1:p.His195Gln
CA150438
NM_000744.7:c.585C>G
CA409637751
NM_000744.7:c.585C>A