Canonical Allele Identifier: PA2826416607
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_001243779.1:p.Gly13226Arg
CA1995602
NM_001256850.1:c.39676G>A
CA349641099
NM_001256850.1:c.39676G>C