Canonical Allele Identifier: PA2830205923
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val28950Ala
CA310953
NM_133378.4:c.86849T>C