Canonical Allele Identifier: PA102123
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_000174.1:p.Asp263Gly
CA341338
NM_000183.3:c.788A>G