Canonical Allele Identifier: PA283934
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_001243779.1:p.Ile26134Val
CA283931
NM_001256850.1:c.78400A>G