Canonical Allele Identifier: PA2830202915
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1314171
ClinVar RCV Id: RCV001771402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met30651Thr
CA349427748
NM_133378.4:c.91952T>C