Canonical Allele Identifier: PA302941
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196643
ClinVar RCV Id: RCV000725273 RCV001086077 RCV001134624 RCV001134621 RCV001134623 RCV002227933 RCV001134620 RCV001134622 RCV002362905 RCV004537431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val30338Ile
CA302940
NM_133378.4:c.91012G>A