Canonical Allele Identifier: PA2580255773
Gene: BAAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2286475
ClinVar RCV Id: RCV004135035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001692.1:p.Leu290Met
CA374254724
NM_001701.4:c.868T>A