Canonical Allele Identifier: PA248767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165813
ClinVar RCV Id: RCV000152207 RCV000273789 RCV000270152 RCV000325455 RCV000364915 RCV000369763 RCV000617421 RCV000471832 RCV000769931 RCV000852807 RCV001530137 RCV004532690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile26901Val
CA248764
NM_001267550.2:c.80701A>G