Canonical Allele Identifier: PA309616
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202568
ClinVar RCV Id: RCV000184443 RCV000218769 RCV000643729 RCV000765584 RCV001134398 RCV001135865 RCV001135867 RCV001135864 RCV001135866 RCV003150065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys9432Glu
CA309614
NM_133378.4:c.28294A>G