Canonical Allele Identifier: PA2826429007
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1761050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33729Ala
CA60953427
NM_001256850.1:c.101185A>G