Canonical Allele Identifier: PA645411794
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405178
ClinVar RCV Id: RCV000458141 RCV000618964 RCV000727768 RCV000765552 RCV001001980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile29150Leu
CA1988318
NM_001267550.2:c.87448A>T
CA349536393
NM_001267550.2:c.87448A>C