Canonical Allele Identifier: PA2830197116
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 978753
ClinVar RCV Id: RCV001293176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro17406Thr
CA1992582
NM_133378.4:c.52216C>A