Canonical Allele Identifier: PA645410700
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404949
ClinVar RCV Id: RCV000476086 RCV001696798 RCV002374750 RCV002265767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr22282His
CA1991411
NM_001267550.2:c.66844T>C