Canonical Allele Identifier: PA302619
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192155
ClinVar RCV Id: RCV000172636 RCV000214788 RCV000467029 RCV001135367 RCV001135368 RCV001135369 RCV001135366 RCV001135365 RCV001798622 RCV002336416
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr23012Lys
CA302618
NM_133378.4:c.69035C>A