Canonical Allele Identifier: PA310757
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_001243779.1:p.Thr27563Arg
CA310756
NM_001256850.1:c.82688C>G