Canonical Allele Identifier: PA139958
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47083
ClinVar RCV Id: RCV000040353 RCV000245658 RCV000231268 RCV000770009 RCV001131772 RCV001131771 RCV001131773 RCV001131774 RCV001132763 RCV001293198 RCV001705688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg18050Cys
CA139954
NM_001267550.2:c.54148C>T