Canonical Allele Identifier: PA311141
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203067
ClinVar RCV Id: RCV000544778 RCV000725232 RCV001844076 RCV002390482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser34219Arg
CA311139
NM_001267550.2:c.102657T>A
CA349417045
NM_001267550.2:c.102657T>G
CA349417051
NM_001267550.2:c.102655A>C