Canonical Allele Identifier: PA284244
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47641
ClinVar RCV Id: RCV000040910 RCV000233206 RCV000245404 RCV000289503 RCV000344458 RCV000341092 RCV000388677 RCV000393835 RCV000769856 RCV000852779 RCV001085578
ClinVar Variation Id: 2105994
ClinVar RCV Id: RCV003023730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gln31354His
CA284242
NM_133378.4:c.94062G>C
CA349419600
NM_133378.4:c.94062G>T