Canonical Allele Identifier: PA139399
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46871
ClinVar RCV Id: RCV000040141 RCV000254304 RCV000725191 RCV001131289 RCV001130561 RCV001131288 RCV001082304 RCV001130562 RCV001130563 RCV001798144 RCV004534890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro10853Ser
CA139397
NM_001267550.2:c.32557C>T