Canonical Allele Identifier: PA310613
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202893
ClinVar RCV Id: RCV000216901 RCV000242789 RCV000462467 RCV000852808 RCV001129610 RCV001129611 RCV001129608 RCV001170792 RCV001129607 RCV001129609 RCV001721163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn26567Ser
CA310611
NM_001267550.2:c.79700A>G