Canonical Allele Identifier: PA174135
Gene: ANO9 HGNC NCBI

Linked Data

ClinVar Variation Id: 161493
ClinVar RCV Id: RCV000149027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012302.2:p.Asp682Glu
CA174134
NM_001012302.3:c.2046C>G
CA378879136
NM_001012302.3:c.2046C>A