Allele Registry

Canonical Allele Identifier: PA915983872

Gene: HMBS HGNC NCBI

ClinVar RCV:

RCV000824246

ClinVar Variation:

665873

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245138.1:p.Arg9Leu	CA382888156 NM_001258209.2:c.26G>T