Canonical Allele Identifier: PA103084
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 1458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Ala55Ser
CA251818
NM_000190.4:c.163G>T