Canonical Allele Identifier: PA1139743029
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 641268
ClinVar RCV Id: RCV000794472
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Gly445Val
CA351608753
NM_001370658.1:c.1334G>T