Canonical Allele Identifier: PA645381371
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val9831Met
CA302465
NM_003319.4:c.29491G>A