Canonical Allele Identifier: PA2827195872
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 2499909
ClinVar RCV Id: RCV003224001
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310511.1:p.Ser299Phe
CA351607571
NM_001323582.1:c.896C>T