Allele Registry

Canonical Allele Identifier: PA103073

Gene: HMBS HGNC NCBI

ClinVar RCV:

RCV000001519

ClinVar Variation:

1454

HGVS (amino-acid)	Matching Registered Transcripts
NP_000181.2:p.Ala31Thr	CA251809 NM_000190.4:c.91G>A