Canonical Allele Identifier: PA183647
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179058
ClinVar RCV Id: RCV000155842 RCV000732240 RCV001085994 RCV002381498 RCV003486702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met4269Thr
CA183646
NM_133432.3:c.12806T>C