Canonical Allele Identifier: PA2825333077
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1030657
ClinVar RCV Id: RCV001332261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Leu75Pro
CA382890512
NM_001024382.2:c.224T>C