Canonical Allele Identifier: PA103488
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 845662
ClinVar RCV Id: RCV001048773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Gly236Ser
CA382897559
NM_000190.4:c.706G>A