Canonical Allele Identifier: PA237633
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg31524His
CA237632
NM_133378.4:c.94571G>A