Canonical Allele Identifier: PA2830193540
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466964

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser7979Pro
CA1999746
NM_133378.4:c.23935T>C