Canonical Allele Identifier: PA139646
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46962
ClinVar RCV Id: RCV000726416 RCV001089291 RCV000040232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1175Thr
CA139643
NM_001267550.2:c.3523G>A