Canonical Allele Identifier: PA138921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46671
ClinVar RCV Id: RCV000039941 RCV000172694 RCV001132883 RCV001079880 RCV001132884 RCV001131917 RCV001131918 RCV001131919 RCV001798134 RCV004534864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu6781Lys
CA138917
NM_001267550.2:c.20341G>A