Canonical Allele Identifier: PA2830193602
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405095
ClinVar RCV Id: RCV000461969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn8133Lys
CA1999655
NM_133378.4:c.24399C>A
CA349440246
NM_133378.4:c.24399C>G