Canonical Allele Identifier: PA181937
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178257
ClinVar RCV Id: RCV000154998 RCV000172703 RCV000621842 RCV000852922 RCV001085765 RCV001798510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val3933Met
CA181936
NM_001256850.1:c.11797G>A