Canonical Allele Identifier: PA139476
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46904
ClinVar RCV Id: RCV000040174 RCV000082392 RCV000309400 RCV000350143 RCV000369677 RCV000315049 RCV000399534 RCV000852870 RCV001082919 RCV001798146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu10221Asp
CA139474
NM_133378.4:c.30663A>C
CA349524450
NM_133378.4:c.30663A>T