Canonical Allele Identifier: PA139316
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46837
ClinVar RCV Id: RCV000040107 RCV000260855 RCV000262132 RCV000253899 RCV000353220 RCV000385979 RCV000300682 RCV000475078 RCV001170630 RCV000725352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr8918Met
CA139313
NM_133378.4:c.26753C>T