Allele Registry

Canonical Allele Identifier: PA2826591811

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021961

ClinVar Variation:

25039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Pro233Ser	CA278256 NM_001281725.2:c.697C>T