Canonical Allele Identifier: PA2830239769
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202990
ClinVar RCV Id: RCV000249807 RCV000315107 RCV000278867 RCV000336224 RCV000373149 RCV000338023 RCV000397381 RCV000397369 RCV000461639 RCV000768859 RCV001084202 RCV001293190 RCV004537559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn22027Ser
CA310908
NM_133437.4:c.66080A>G