Canonical Allele Identifier: PA2573164261
Gene: HADHB HGNC NCBI

Linked Data

ClinVar Variation Id: 1494677
ClinVar RCV Id: RCV001989526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000174.1:p.Ala232Ser
CA346092960
NM_000183.3:c.694G>T