ClinGen Allele Registry
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Canonical Allele Identifier:
PA916048672
Gene: BTD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
36382
ClinVar RCV:
RCV000021967
RCV001251702
ClinVar Variation:
25045
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001357681.1:p.Leu258Pro
CA278266
NM_001370752.1:c.773T>C