Canonical Allele Identifier: PA237857
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu22441Gly
CA237855
NM_001267550.2:c.67322A>G