Allele Registry

Canonical Allele Identifier: PA2828445899

Gene: BTD HGNC NCBI

ClinVar Allele:

36363

ClinVar RCV:

RCV000021947

RCV000985649

RCV003415728

ClinVar Variation:

25026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357587.1:p.Val179Met	CA278235 NM_001370658.1:c.535G>A