Canonical Allele Identifier: PA2830206261
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132135
ClinVar RCV Id: RCV000119023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Trp29161Leu
CA358824
NM_133378.4:c.87482G>T