Canonical Allele Identifier: PA2828446025
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25048
ClinVar RCV Id: RCV001310478 RCV003323364 RCV003497832
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357587.1:p.Val276Gly
CA278272
NM_001370658.1:c.827T>G