Canonical Allele Identifier: PA645412734
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229569
ClinVar RCV Id: RCV000215601 RCV000318098 RCV000278285 RCV000335727 RCV000375123 RCV000404751 RCV001722172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34638His
CA1985523
NM_001267550.2:c.103913G>A