Allele Registry

Canonical Allele Identifier: PA2826454735

Gene: HMBS HGNC NCBI

ClinVar RCV:

RCV001216002

ClinVar Variation:

945373

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245137.1:p.Arg26Pro	CA382888155 NM_001258208.2:c.77G>C