Canonical Allele Identifier: PA141411
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47579
ClinVar RCV Id: RCV000040848 RCV000185032 RCV000242748 RCV001130310 RCV001135351 RCV001135352 RCV001135353 RCV001135354 RCV001798203 RCV001085595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30726Cys
CA141408
NM_001256850.1:c.92176C>T