Canonical Allele Identifier: PA139620
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46955
ClinVar RCV Id: RCV000040225 RCV000172337 RCV000294831 RCV000328437 RCV000343733 RCV000383259 RCV000399696 RCV000618332 RCV001079995 RCV002225277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val11542Ala
CA139618
NM_133378.4:c.34625T>C