Canonical Allele Identifier: PA302597
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192135
ClinVar RCV Id: RCV000172600 RCV000222652 RCV000266936 RCV000266285 RCV000301237 RCV000246902 RCV000380571 RCV000321269 RCV000469383 RCV000769843 RCV001563645 RCV004535177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu35559Gln
CA302594
NM_001267550.2:c.106675G>C