Canonical Allele Identifier: PA313467
Gene: CHRNA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 204972
ClinVar RCV Id: RCV000186877 RCV001302866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000733.2:p.Leu389Phe
CA313466
NM_000742.4:c.1165C>T