Canonical Allele Identifier: PA2830220925
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr18013Met
CA183467
NM_133432.3:c.54038C>T