Canonical Allele Identifier: PA2826422152
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467478
ClinVar RCV Id: RCV000543490 RCV002341351 RCV000733724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala23446Thr
CA1990080
NM_001256850.1:c.70336G>A