Canonical Allele Identifier: PA2830210627
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met1233Leu
CA311304
NM_133432.3:c.3697A>T
CA349477727
NM_133432.3:c.3697A>C