Canonical Allele Identifier: PA309628
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202572
ClinVar RCV Id: RCV000466533 RCV001721153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile10887Thr
CA309626
NM_001267550.2:c.32660T>C