Canonical Allele Identifier: PA2830204018
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1502498
ClinVar RCV Id: RCV002011008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.His32256Tyr
CA349411644
NM_133378.4:c.96766C>T