Canonical Allele Identifier: PA658806127
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Gly632Asp
CA2005945
NM_133379.5:c.1895G>A