Canonical Allele Identifier: PA140143
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu19773Gly
CA140139
NM_001267550.2:c.59318A>G