Canonical Allele Identifier: PA645412555
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229557
ClinVar RCV Id: RCV000215975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro33314Ser
CA1986105
NM_001267550.2:c.99940C>T