Canonical Allele Identifier: PA141269
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47525
ClinVar RCV Id: RCV000040794 RCV000714120 RCV000768860 RCV000852788 RCV001082181 RCV001129729 RCV001132439 RCV001132436 RCV001132437 RCV001132438 RCV002362647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val30846Ala
CA141265
NM_001267550.2:c.92537T>C