Canonical Allele Identifier: PA141092
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47465
ClinVar RCV Id: RCV000040734 RCV000225888 RCV000244493 RCV000726191 RCV001129285 RCV001136274 RCV001136271 RCV001136272 RCV001136273 RCV001798190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr27567Phe
CA141089
NM_001256850.1:c.82700A>T