Canonical Allele Identifier: PA658814285
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_001254479.2:p.Gly16284Arg
CA1994734
NM_001267550.2:c.48850G>A
CA349607731
NM_001267550.2:c.48850G>C