Canonical Allele Identifier: PA140621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47302
ClinVar RCV Id: RCV000040572 RCV000172643 RCV000252755 RCV000263162 RCV000374141 RCV000315908 RCV000330895 RCV000370274 RCV001079127 RCV000768933 RCV001781363 RCV004534925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile23902Thr
CA140617
NM_001267550.2:c.71705T>C