Canonical Allele Identifier: PA658666144
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467325
ClinVar RCV Id: RCV000545524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg19780Ser
CA349494156
NM_001267550.2:c.59340G>T
CA349494157
NM_001267550.2:c.59340G>C