Canonical Allele Identifier: PA251835
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1473
ClinVar RCV Id: RCV000001538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Ala235Val
CA251834
NM_001024382.2:c.704C>T