Canonical Allele Identifier: PA2826588188
Gene: HADHB HGNC NCBI

Linked Data

ClinVar Variation Id: 14844
ClinVar RCV Id: RCV003156214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268441.1:p.Asp248Gly
CA341338
NM_001281512.2:c.743A>G