Canonical Allele Identifier: PA139120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46752
ClinVar RCV Id: RCV000040022 RCV000118744 RCV001087646 RCV004541139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala7119Ser
CA139118
NM_133378.4:c.21355G>T