Allele Registry

Canonical Allele Identifier: PA2826589509

Gene: BTD HGNC NCBI

ClinVar Allele:

36327

ClinVar RCV:

RCV000021907

RCV001171830

RCV001800312

ClinVar Variation:

24989

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Ala62Val	CA278170 NM_001281723.3:c.185C>T