Canonical Allele Identifier: PA916063383
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val9956Met
CA302465
NM_133432.3:c.29866G>A