Canonical Allele Identifier: PA302951
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196725
ClinVar RCV Id: RCV000213075 RCV000547954 RCV000724101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val35864Ala
CA302948
NM_001267550.2:c.107591T>C