Canonical Allele Identifier: PA916065761
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47016
ClinVar RCV Id: RCV000040286 RCV000227469 RCV000337139 RCV000285222 RCV000342472 RCV000302752 RCV000391758 RCV000621575 RCV000769005 RCV001085025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Leu7040Phe
CA283315
NM_133437.4:c.21118C>T