Canonical Allele Identifier: PA2830215415
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.His8625Asp
CA310025
NM_133432.3:c.25873C>G