Allele Registry

Canonical Allele Identifier: PA2826455058

Gene: HMBS HGNC NCBI

ClinVar RCV:

RCV000430573

ClinVar Variation:

381651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245138.1:p.Val210Met	CA16606875 NM_001258209.2:c.628G>A