Canonical Allele Identifier: PA645381902
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404735
ClinVar RCV Id: RCV000468033 RCV002480351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Met113Val
CA16610652
NM_133379.5:c.337A>G