Canonical Allele Identifier: PA138990
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46696
ClinVar RCV Id: RCV000039966 RCV000643520 RCV003486574 RCV002477118 RCV001573334 RCV003319175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg6120Trp
CA138988
NM_133378.4:c.18358C>T