Canonical Allele Identifier: PA238273
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.His1952Arg
CA238269
NM_133379.5:c.5855A>G