Canonical Allele Identifier: PA181692
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96309
ClinVar RCV Id: RCV000154911 RCV000231904 RCV000621416 RCV000852803 RCV001130751 RCV001130753 RCV001133725 RCV001130750 RCV001130752 RCV001811389 RCV003486644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr26273Ala
CA181689
NM_001256850.1:c.78817A>G