Canonical Allele Identifier: PA645410476
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332817
ClinVar RCV Id: RCV000281500 RCV000293984 RCV000338846 RCV000351260 RCV000386335 RCV001565788 RCV002450899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu20457Ala
CA1992378
NM_001267550.2:c.61370A>C