Canonical Allele Identifier: PA311869
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203268
ClinVar RCV Id: RCV000185356 RCV000543023 RCV000726954 RCV002274948 RCV003486763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg5741Cys
CA311868
NM_001256850.1:c.17221C>T