Canonical Allele Identifier: PA1139679829
Gene: HADHB HGNC NCBI

Linked Data

ClinVar Variation Id: 894831
ClinVar RCV Id: RCV001136588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000174.1:p.Glu448Gly
CA44342947
NM_000183.3:c.1343A>G