Canonical Allele Identifier: PA2580402316
Gene: CHRNA9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2370961
ClinVar RCV Id: RCV004207750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060051.2:p.Val467Ala
CA2898194
NM_017581.4:c.1400T>C