Canonical Allele Identifier: PA916065329
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332867
ClinVar RCV Id: RCV000271481 RCV000277289 RCV000328849 RCV000363601 RCV000376613 RCV000732908 RCV001479457 RCV003317194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly5994Arg
CA1995602
NM_133437.4:c.17980G>A
CA349641099
NM_133437.4:c.17980G>C