Canonical Allele Identifier: PA311017
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203026
ClinVar RCV Id: RCV000291952 RCV000345460 RCV000398371 RCV000381427 RCV000469120 RCV000311155 RCV000346821 RCV002372136 RCV001721174 RCV001844075 RCV004537562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser30775Leu
CA311016
NM_001256850.1:c.92324C>T