Canonical Allele Identifier: PA2830204013
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1025007
ClinVar RCV Id: RCV001325263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32250del
CA1985425
NM_133378.4:c.96748_96750del