Canonical Allele Identifier: PA658816239
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535366
ClinVar RCV Id: RCV000643302 RCV000825689 RCV000852804 RCV001085404 RCV001293123 RCV004533357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe27758Leu
CA1988949
NM_001267550.2:c.83272T>C
CA349568519
NM_001267550.2:c.83274T>A
CA349568522
NM_001267550.2:c.83274T>G