Canonical Allele Identifier: PA237682
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191843
ClinVar RCV Id: RCV000172184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp32013His
CA237680
NM_001267550.2:c.96037G>C