Canonical Allele Identifier: PA140132
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47146
ClinVar RCV Id: RCV000040416 RCV000469250 RCV000491963 RCV000725816 RCV000852513 RCV002321523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg18064Cys
CA140129
NM_001256850.1:c.54190C>T