Canonical Allele Identifier: PA2826491201
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229568
ClinVar RCV Id: RCV000218560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val321Ile
CA10576582
NM_001267550.2:c.961G>A