Canonical Allele Identifier: PA2830237008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202893
ClinVar RCV Id: RCV000216901 RCV000242789 RCV000462467 RCV000852808 RCV001129610 RCV001129611 RCV001129608 RCV001170792 RCV001129607 RCV001129609 RCV001721163
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn17694Ser
CA310611
NM_133437.4:c.53081A>G