Canonical Allele Identifier: PA2826422205
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1329195
ClinVar RCV Id: RCV001799238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu23551Gly
CA60995088
NM_001256850.1:c.70652A>G