Canonical Allele Identifier: PA2830209079
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1034511
ClinVar RCV Id: RCV001337245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val32241Leu
CA1985429
NM_133378.4:c.96721G>C
CA349411760
NM_133378.4:c.96721G>T