Allele Registry

Canonical Allele Identifier: PA2826454732

Gene: HMBS HGNC NCBI

ClinVar RCV:

RCV000824246

ClinVar Variation:

665873

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245137.1:p.Arg26Leu	CA382888156 NM_001258208.2:c.77G>T