Canonical Allele Identifier: PA2830192141
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser4207Gly
CA2002044
NM_133378.4:c.12619A>G