Canonical Allele Identifier: PA645412820
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405037
ClinVar RCV Id: RCV000476896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35166Val
CA16610295
NM_001267550.2:c.105497G>T