Canonical Allele Identifier: PA358825
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_001254479.2:p.Trp31729Leu
CA358824
NM_001267550.2:c.95186G>T