Canonical Allele Identifier: PA302378
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191809
ClinVar RCV Id: RCV000172148 RCV001132849 RCV001132848 RCV001132850 RCV001347072 RCV001132847 RCV001136253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg35448Gln
CA302375
NM_001267550.2:c.106343G>A