Canonical Allele Identifier: PA2826454772
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245137.1:p.Arg116Trp
CA251793
NM_001258208.2:c.346C>T