Canonical Allele Identifier: PA283935
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47425
ClinVar RCV Id: RCV000040694 RCV000247992 RCV000296101 RCV000381205 RCV000350969 RCV000351181 RCV000406850 RCV000993496 RCV001513447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile27775Val
CA283931
NM_001267550.2:c.83323A>G