Canonical Allele Identifier: PA2830224246
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val23066Met
CA310995
NM_133432.3:c.69196G>A