Canonical Allele Identifier: PA916065776
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser7073Pro
CA309899
NM_133437.4:c.21217T>C