Canonical Allele Identifier: PA141239
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47514
ClinVar RCV Id: RCV000040783 RCV000082447 RCV000621123 RCV000852791 RCV001082275 RCV001130053 RCV001135074 RCV001135075 RCV001135076 RCV001135077 RCV001798197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala28948Thr
CA141236
NM_001256850.1:c.86842G>A