Canonical Allele Identifier: PA141325
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47549
ClinVar RCV Id: RCV000040818 RCV000765538 RCV000726197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly30054Arg
CA141322
NM_001256850.1:c.90160G>A
CA349466615
NM_001256850.1:c.90160G>C