Canonical Allele Identifier: PA2826591705
Gene: BTD HGNC NCBI

Linked Data

ClinVar Variation Id: 25026
ClinVar RCV Id: RCV000021947 RCV000985649 RCV003415728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268654.1:p.Val179Met
CA278235
NM_001281725.2:c.535G>A