Canonical Allele Identifier: PA2829443677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile23995Leu
CA1986243
NM_003319.4:c.71983A>C
CA349430779
NM_003319.4:c.71983A>T