Canonical Allele Identifier: PA2580056768
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1957595
ClinVar RCV Id: RCV002690744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Ile110Val
CA382891043
NM_000190.4:c.328A>G