Canonical Allele Identifier: PA311206
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203089
ClinVar RCV Id: RCV000185112 RCV002516954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33376Ala
CA311205
NM_001256850.1:c.100126A>G