Canonical Allele Identifier: PA102082
Gene: HADHB HGNC NCBI

Linked Data

ClinVar Variation Id: 14847
ClinVar RCV Id: RCV003156217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000174.1:p.Arg444Lys
CA341341
NM_000183.3:c.1331G>A