Canonical Allele Identifier: PA2830234998
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser14255Tyr
CA202117
NM_133437.4:c.42764C>A