ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826592185
Gene: BTD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
25082
ClinVar RCV Id:
RCV000022007
RCV000985644
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001268654.1:p.Gly425Val
CA278330
NM_001281725.2:c.1274G>T