Canonical Allele Identifier: PA2826647107
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_001269384.1:p.Cys358Ser
CA4689523
NM_001282455.2:c.1073G>C
CA370809443
NM_001282455.2:c.1072T>A