Canonical Allele Identifier: PA2828538767
Gene: BAAT HGNC NCBI

Linked Data

ClinVar Variation Id: 21301
ClinVar RCV Id: RCV000020464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361644.1:p.Ile323Val
CA341872
NM_001374715.1:c.967A>G