Canonical Allele Identifier: PA138846
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46644
ClinVar RCV Id: RCV000039914 RCV000229581 RCV000246252 RCV000283432 RCV000289663 RCV000380242 RCV000340760 RCV000341928 RCV000852902 RCV001080584 RCV001170640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr5942Ser
CA138843
NM_001256850.1:c.17825C>G
CA349559844
NM_001256850.1:c.17824A>T