Canonical Allele Identifier: PA139435
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46883
ClinVar RCV Id: RCV000040153 RCV000244280 RCV000540453 RCV000725326 RCV000770061 RCV000852874 RCV001130927 RCV001130929 RCV001130926 RCV001130928 RCV001130925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr9776Cys
CA139431
NM_133378.4:c.29327A>G