Canonical Allele Identifier: PA2830206317
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203281
ClinVar RCV Id: RCV000220599 RCV000469447 RCV000852898 RCV004537570 RCV003137756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr5397Asn
CA311907
NM_133378.4:c.16190C>A