Canonical Allele Identifier: PA2830207627
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 440367
ClinVar RCV Id: RCV000508163 RCV001130358 RCV001130354 RCV001130355 RCV001130356 RCV001130357 RCV002481644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val8088Met
CA1999678
NM_133378.4:c.24262G>A