Canonical Allele Identifier: PA2826591992
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 975025
ClinVar RCV Id: RCV001251432

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Phe341Val
CA351608028
NM_001281725.2:c.1021T>G