Canonical Allele Identifier: PA310791
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202952
ClinVar RCV Id: RCV000223660 RCV000301842 RCV000307858 RCV000359092 RCV000404508 RCV000526235 RCV000396053 RCV000727677 RCV000509283 RCV002354516 RCV004537558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg27933Cys
CA310790
NM_001256850.1:c.83797C>T