Canonical Allele Identifier: PA2826429097
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2072287
ClinVar RCV Id: RCV002949529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu33827Val
CA349405502
NM_001256850.1:c.101479C>G