Canonical Allele Identifier: PA2826412039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229594
ClinVar RCV Id: RCV000213210 RCV000643855 RCV001697191 RCV002450638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys3866Glu
CA2002698
NM_001256850.1:c.11596A>G