Canonical Allele Identifier: PA2830204515
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2072287
ClinVar RCV Id: RCV002949529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu32900Val
CA349405502
NM_133378.4:c.98698C>G