Canonical Allele Identifier: PA310228
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202769
ClinVar RCV Id: RCV000643775 RCV000997432 RCV001131031 RCV001133991 RCV001133992 RCV001133993 RCV001133994 RCV002336480 RCV003150069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg19396Cys
CA310227
NM_001256850.1:c.58186C>T