Canonical Allele Identifier: PA211913
Gene: BHLHA9 HGNC NCBI

Linked Data

ClinVar Variation Id: 162066
ClinVar RCV Id: RCV000149487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157877.1:p.Arg73Pro
CA211912
NM_001164405.2:c.218G>C