Canonical Allele Identifier: PA141179
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47493
ClinVar RCV Id: RCV000040762 RCV000458878 RCV000733290 RCV003147329 RCV002362639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val29983Met
CA141176
NM_001267550.2:c.89947G>A