Canonical Allele Identifier: PA1139679808
Gene: HADHB HGNC NCBI

Linked Data

ClinVar Variation Id: 894830
ClinVar RCV Id: RCV001136587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000174.1:p.Arg446Trp
CA1560517
NM_000183.3:c.1336C>T