Canonical Allele Identifier: PA310088
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202722
ClinVar RCV Id: RCV000184634 RCV000727777 RCV001087244 RCV002433827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro18360Leu
CA310086
NM_001267550.2:c.55079C>T