Canonical Allele Identifier: PA2826419028
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467311
ClinVar RCV Id: RCV000547341 RCV001129849 RCV001134841 RCV001134842 RCV001134843 RCV001129850 RCV002491045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser17826Thr
CA60971692
NM_001256850.1:c.53476T>A