Canonical Allele Identifier: PA2830202875
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332707
ClinVar RCV Id: RCV000309603 RCV000285084 RCV000340060 RCV000392740 RCV001288587 RCV000404248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys30571Glu
CA1986187
NM_133378.4:c.91711A>G