Canonical Allele Identifier: PA2829433608
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val7536Leu
CA1994514
NM_003319.4:c.22606G>T
CA349600959
NM_003319.4:c.22606G>C