Canonical Allele Identifier: PA2830230338
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Lys3238Arg
CA311567
NM_133437.4:c.9713A>G