Canonical Allele Identifier: PA658666702
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467426
ClinVar RCV Id: RCV000547446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro23374Ala
CA349664840
NM_001267550.2:c.70120C>G