Canonical Allele Identifier: PA916061487
Gene: TTLL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 778926
ClinVar RCV Id: RCV000959660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114155.4:p.Val559Ile
CA4097587
NM_031949.5:c.1675G>A