Canonical Allele Identifier: PA211911
Gene: BHLHA9 HGNC NCBI

Linked Data

ClinVar Variation Id: 162065
ClinVar RCV Id: RCV000149486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157877.1:p.Asn71Asp
CA211910
NM_001164405.2:c.211A>G