Canonical Allele Identifier: PA2827195808
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 801946
ClinVar RCV Id: RCV000987132
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310511.1:p.Ile235Met
CA351607143
NM_001323582.1:c.705C>G