Canonical Allele Identifier: PA2830208782
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202942
ClinVar RCV Id: RCV000184921 RCV000246125 RCV000727722 RCV001086279 RCV004539725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr26636Arg
CA310756
NM_133378.4:c.79907C>G