Canonical Allele Identifier: PA289097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130670
ClinVar RCV Id: RCV000118764 RCV000253770 RCV000532684 RCV001133286 RCV001133285 RCV001133287 RCV001133288 RCV001133289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp14812Val
CA289095
NM_133378.4:c.44435A>T