Canonical Allele Identifier: PA282638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46578
ClinVar RCV Id: RCV000039848 RCV000205174 RCV000249819 RCV001134669 RCV001134671 RCV001134673 RCV001528575 RCV001134670 RCV001134672 RCV003486570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg3367Gln
CA282632
NM_133379.5:c.10100G>A