Canonical Allele Identifier: PA2830202359
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg29490Trp
CA1986809
NM_133378.4:c.88468C>T