Canonical Allele Identifier: PA141751
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47705
ClinVar RCV Id: RCV000040974
ClinVar Variation Id: 1394513
ClinVar RCV Id: RCV001884827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35482Ser
CA141748
NM_001267550.2:c.106445C>G
CA349405236
NM_001267550.2:c.106444A>T