Canonical Allele Identifier: PA2830195607
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535028
ClinVar RCV Id: RCV000642785 RCV001131286 RCV001131285 RCV001131287 RCV001131283 RCV001131284 RCV001805774 RCV002424456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly13716Arg
CA1994734
NM_133378.4:c.41146G>A
CA349607731
NM_133378.4:c.41146G>C