Canonical Allele Identifier: PA2826426021
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser30077Ile
CA1986997
NM_001256850.1:c.90230G>T