Canonical Allele Identifier: PA645463164
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 343909
ClinVar RCV Id: RCV000262752 RCV000437667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000051.1:p.Asp368Ala
CA10615137
NM_000060.4:c.1103A>C