Canonical Allele Identifier: PA139400
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_596869.4:p.Pro9609Ser
CA139397
NM_133378.4:c.28825C>T