Canonical Allele Identifier: PA916001219
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 661657
ClinVar RCV Id: RCV000819126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp35353Asn
CA349407130
NM_001267550.2:c.106057G>A