Canonical Allele Identifier: PA2829441924
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly21476Arg
CA141232
NM_003319.4:c.64426G>A
CA349499579
NM_003319.4:c.64426G>C