Canonical Allele Identifier: PA2830209332
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192180
ClinVar RCV Id: RCV000172733 RCV000218176 RCV000469634 RCV001140835 RCV001140836 RCV001142683 RCV001170882 RCV001142681 RCV001142682 RCV002326949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val15Ile
CA238531
NM_133432.3:c.43G>A