Canonical Allele Identifier: PA2830243565
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1197339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr26577Ser
CA1985126
NM_133437.4:c.79730C>G
CA349405967
NM_133437.4:c.79729A>T