Canonical Allele Identifier: PA311372
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203133
ClinVar RCV Id: RCV000185166 RCV000642940 RCV000729514 RCV003486761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg1664Trp
CA311369
NM_001267550.2:c.4990C>T