Canonical Allele Identifier: PA2826498047
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229449
ClinVar RCV Id: RCV000216081 RCV000253790 RCV000725245 RCV000852848 RCV001085087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro16920Ala
CA1994319
NM_001267550.2:c.50758C>G