Allele Registry

Canonical Allele Identifier: PA2827195998

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV002651650

ClinVar Variation:

2203322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.Val437Met	CA278335 NM_001323582.1:c.1309G>A