Canonical Allele Identifier: PA915965532
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 659018
ClinVar RCV Id: RCV000815951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Val353Ile
CA229597443
NM_000190.4:c.1057G>A