Canonical Allele Identifier: PA141650
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47664
ClinVar RCV Id: RCV000040933 RCV000475599 RCV001170290 RCV001576785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32081Gln
CA141648
NM_133378.4:c.96242G>A