Canonical Allele Identifier: PA179333
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166320
ClinVar RCV Id: RCV000152506 RCV000172729 RCV000230032 RCV000852937 RCV001132892 RCV001132893 RCV000769129 RCV001131924 RCV001131925 RCV001131926 RCV002326877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Phe1466Leu
CA179328
NM_133379.5:c.4396T>C
CA349469144
NM_133379.5:c.4398C>G
CA349469147
NM_133379.5:c.4398C>A