Canonical Allele Identifier: PA140652
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47313
ClinVar RCV Id: RCV000040583 RCV000460260 RCV000620443 RCV000723985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met24061Thr
CA140649
NM_001267550.2:c.72182T>C