Canonical Allele Identifier: PA658664879
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466876
ClinVar RCV Id: RCV000557256 RCV001131913 RCV001131915 RCV001131916 RCV001131912 RCV001131914 RCV003139782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser6785Leu
CA2001223
NM_001267550.2:c.20354C>T