Canonical Allele Identifier: PA2826454718
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 2846906
ClinVar RCV Id: RCV003690529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245137.1:p.Ala11Val
CA382985835
NM_001258208.2:c.32C>T