Canonical Allele Identifier: PA2825333213
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1399638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Ala232Thr
CA6314169
NM_001024382.2:c.694G>A