Canonical Allele Identifier: PA2826409906
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met113Val
CA16610652
NM_001256850.1:c.337A>G