Canonical Allele Identifier: PA2826420598
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47244
ClinVar RCV Id: RCV000040514 RCV000727127 RCV000621653 RCV001087265 RCV001170578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile20665Thr
CA140437
NM_001256850.1:c.61994T>C