Canonical Allele Identifier: PA645409994
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16339Trp
CA1994704
NM_001267550.2:c.49015C>T