Canonical Allele Identifier: PA2826416752
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405183
ClinVar RCV Id: RCV000465470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg13556Gly
CA1995414
NM_001256850.1:c.40666A>G