Canonical Allele Identifier: PA103824
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 381651
ClinVar RCV Id: RCV000430573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Val267Met
CA16606875
NM_000190.4:c.799G>A