Canonical Allele Identifier: PA2830197169
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp17547Asn
CA1992502
NM_133378.4:c.52639G>A