Canonical Allele Identifier: PA140141
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47149
ClinVar RCV Id: RCV000040419 RCV000172655 RCV001085920 RCV002321525 RCV004541163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu17205Gly
CA140139
NM_133378.4:c.51614A>G