Canonical Allele Identifier: PA139392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46868
ClinVar RCV Id: RCV000040138 RCV000082390 RCV001131295 RCV001134271 RCV001086201 RCV001134272 RCV001134273 RCV001134274 RCV003486581 RCV004534889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala10510Val
CA139390
NM_001256850.1:c.31529C>T