Canonical Allele Identifier: PA2829439136
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202889
ClinVar RCV Id: RCV000184854 RCV000529796 RCV001721162 RCV002345655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr17084Ser
CA310599
NM_003319.4:c.51251C>G
CA349602915
NM_003319.4:c.51250A>T