Canonical Allele Identifier: PA139411
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46873
ClinVar RCV Id: RCV000040143 RCV000118748 RCV000245813 RCV000852875 RCV000770067 RCV001134134 RCV001134135 RCV001134137 RCV001081904 RCV001134136 RCV001134138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro9631Leu
CA139407
NM_133378.4:c.28892C>T