Canonical Allele Identifier: PA2825333042
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 2137262
ClinVar RCV Id: RCV003062462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Leu25Ser
CA382888459
NM_001024382.2:c.74T>C