Canonical Allele Identifier: PA140207
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47168
ClinVar RCV Id: RCV000040438 RCV000233759 RCV000242716 RCV000768968 RCV001136053 RCV001136054 RCV001136055 RCV001136056 RCV001136057 RCV001082822 RCV004534914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg18726Gln
CA140204
NM_001256850.1:c.56177G>A