Canonical Allele Identifier: PA2826142441
Gene: HADH HGNC NCBI

Linked Data

ClinVar Variation Id: 8019
ClinVar RCV Id: RCV000008483 RCV001762038 RCV003221347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171634.3:p.Asp57Glu
CA119223
NM_001184705.4:c.171C>A
CA357830703
NM_001184705.4:c.171C>G