Canonical Allele Identifier: PA2830230935
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp4396Glu
CA238155
NM_133437.4:c.13188T>G
CA349606837
NM_133437.4:c.13188T>A