Canonical Allele Identifier: PA310600
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_001243779.1:p.Thr24508Ser
CA310599
NM_001256850.1:c.73523C>G
CA349602915
NM_001256850.1:c.73522A>T