Canonical Allele Identifier: PA2829441863
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly21386Asp
CA310872
NM_003319.4:c.64157G>A