Canonical Allele Identifier: PA2741994362
Gene: TTLL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2527632
ClinVar RCV Id: RCV004300930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114155.4:p.Phe562Leu
CA366425085
NM_031949.5:c.1684T>C
CA366425090
NM_031949.5:c.1686C>A
CA366425091
NM_031949.5:c.1686C>G