Canonical Allele Identifier: PA2580055816
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1477603
ClinVar RCV Id: RCV002018786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Lys98Glu
CA382890641
NM_000190.4:c.292A>G