Canonical Allele Identifier: PA251814
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019553.1:p.Arg150Trp
CA251813
NM_001024382.2:c.448C>T