Canonical Allele Identifier: PA2826416532
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1778491
ClinVar RCV Id: RCV002398830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val13118Phe
CA349645132
NM_001256850.1:c.39352G>T