Canonical Allele Identifier: PA2825333257
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1720756
ClinVar RCV Id: RCV002305218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Leu298Ser
CA382899205
NM_001024382.2:c.893T>C