Canonical Allele Identifier: PA645412192
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser31718Ile
CA1986997
NM_001267550.2:c.95153G>T