Canonical Allele Identifier: PA2741849698
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2944821
ClinVar RCV Id: RCV003808523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn35348Thr
CA349407155
NM_001267550.2:c.106043A>C