Canonical Allele Identifier: PA658666536
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467392
ClinVar RCV Id: RCV000550774 RCV000607451 RCV000727753 RCV001170579 RCV002377097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val22235Ile
CA1991458
NM_001267550.2:c.66703G>A