Canonical Allele Identifier: PA2826454941
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 2832305
ClinVar RCV Id: RCV003689432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245138.1:p.Val73Ala
CA382890378
NM_001258209.2:c.218T>C