Canonical Allele Identifier: PA2826427035
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_001243779.1:p.Met31578Thr
CA349427748
NM_001256850.1:c.94733T>C