Canonical Allele Identifier: PA658665586
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467172
ClinVar RCV Id: RCV000531429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro15390Leu
CA60993148
NM_001267550.2:c.46169C>T