Canonical Allele Identifier: PA311234
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203098
ClinVar RCV Id: RCV000459954 RCV000997317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg35164His
CA311232
NM_001267550.2:c.105491G>A