Canonical Allele Identifier: PA139611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46949
ClinVar RCV Id: RCV000040219 RCV000172731 RCV000250640 RCV000852941 RCV001084204 RCV001129652 RCV001129653 RCV001129654 RCV001129655 RCV001132367 RCV001798150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly1137Arg
CA139607
NM_001267550.2:c.3409G>C