Canonical Allele Identifier: PA139292
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46824
ClinVar RCV Id: RCV000040094 RCV000643692 RCV000725042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr869Ser
CA139287
NM_133378.4:c.2605A>T
CA349496328
NM_133378.4:c.2606C>G