Canonical Allele Identifier: PA645382992
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229444
ClinVar RCV Id: RCV000221874 RCV000532189 RCV000617303 RCV001697190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ile1361Leu
CA2005411
NM_133379.5:c.4081A>C