Canonical Allele Identifier: PA2826428976
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2944821
ClinVar RCV Id: RCV003808523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn33707Thr
CA349407155
NM_001256850.1:c.101120A>C