Canonical Allele Identifier: PA141199
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47501
ClinVar RCV Id: RCV000040770 RCV000082445 RCV000286969 RCV000278620 RCV000327591 RCV000376846 RCV000373393 RCV000618823 RCV000852794 RCV001083184 RCV001798195 RCV003993769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Cys27708Gly
CA141197
NM_133378.4:c.83122T>G