Canonical Allele Identifier: PA916066872
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Met9374Thr
CA302473
NM_133437.4:c.28121T>C