Canonical Allele Identifier: PA138721
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46599
ClinVar RCV Id: RCV000039869 RCV000277012 RCV000245443 RCV000273361 RCV000331058 RCV000356589 RCV000369337 RCV000416068 RCV001079457 RCV000769081 RCV000852913 RCV002227928 RCV003993764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val3816Leu
CA138719
NM_133378.4:c.11446G>C