Canonical Allele Identifier: PA916066192
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 377167
ClinVar RCV Id: RCV000441173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile7810Asn
CA16603286
NM_133437.4:c.23429T>A