Canonical Allele Identifier: PA2826590912
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 156004
ClinVar RCV Id: RCV000144061 RCV000494587
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268653.2:p.Asn280His
CA278441
NM_001281724.3:c.838A>C