Canonical Allele Identifier: PA139742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47005
ClinVar RCV Id: RCV000040275 RCV000724839 RCV001078812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu15608Ser
CA139739
NM_001267550.2:c.46823T>C