Allele Registry

Canonical Allele Identifier: PA2826591119

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000032020

RCV003480039

ClinVar Variation:

38577

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.Gly393Ser	CA278392 NM_001281724.3:c.1177G>A