Canonical Allele Identifier: PA283462
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47105
ClinVar RCV Id: RCV000040375 RCV000228188 RCV000620720 RCV001134251 RCV001131279 RCV001134253 RCV001085000 RCV001134252 RCV001134254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile15948Thr
CA283460
NM_133378.4:c.47843T>C