Canonical Allele Identifier: PA310008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202695
ClinVar RCV Id: RCV000184601 RCV000852846 RCV001085392 RCV003987430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg15594Gln
CA310007
NM_001256850.1:c.46781G>A