Canonical Allele Identifier: PA2830193608
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1315137
ClinVar RCV Id: RCV001773331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser8137Cys
CA1999653
NM_133378.4:c.24410C>G