Canonical Allele Identifier: PA916065631
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467181
ClinVar RCV Id: RCV000541917 RCV001564240 RCV002413549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly6658Arg
CA1995217
NM_133437.4:c.19972G>A
CA60991509
NM_133437.4:c.19972G>C