Canonical Allele Identifier: PA916064261
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala63Thr
CA311611
NM_133437.4:c.187G>A