Canonical Allele Identifier: PA103379
Gene: HMBS HGNC NCBI

Linked Data

ClinVar Variation Id: 2137264
ClinVar RCV Id: RCV003062464

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000181.2:p.Glu209Lys
CA229596005
NM_000190.4:c.625G>A