Canonical Allele Identifier: PA2829136661
Gene: PATL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444051
ClinVar RCV Id: RCV000512631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001374189.1:p.Ile287Thr
CA270118879
NM_001387260.1:c.860T>C