Canonical Allele Identifier: PA658808974
Gene: BHLHA9 HGNC NCBI

Linked Data

ClinVar Variation Id: 501415
ClinVar RCV Id: RCV000596561 RCV002531085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157877.1:p.Ala39Glu
CA286778989
NM_001164405.2:c.116C>A