Canonical Allele Identifier: PA2826415413
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro10949Ser
CA178903
NM_001256850.1:c.32845C>T