Canonical Allele Identifier: PA645444920
Gene: CHRNA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421771
ClinVar RCV Id: RCV000486276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000733.2:p.Cys373Ser
CA4689523
NM_000742.4:c.1118G>C
CA370809443
NM_000742.4:c.1117T>A