Canonical Allele Identifier: PA916066836
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Tyr9291His
CA139980
NM_133437.4:c.27871T>C