Canonical Allele Identifier: PA311176
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203079
ClinVar RCV Id: RCV000185101 RCV002399689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu33144Gln
CA311175
NM_001256850.1:c.99430G>C