Canonical Allele Identifier: PA141317
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47545
ClinVar RCV Id: RCV000040814 RCV000252550 RCV000513556 RCV001082680 RCV000768854 RCV001131865 RCV001132851 RCV001131864 RCV001131866 RCV001131867 RCV004534941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp31617Glu
CA141313
NM_001267550.2:c.94851T>A
CA349469525
NM_001267550.2:c.94851T>G