Canonical Allele Identifier: PA139511
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46914
ClinVar RCV Id: RCV000040184 RCV000246293 RCV000274824 RCV000329904 RCV000364890 RCV000370805 RCV000389983 RCV000464829 RCV000769035 RCV001293076 RCV001719766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys11381Thr
CA139508
NM_001256850.1:c.34142A>C