Canonical Allele Identifier: PA2826415536
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro11205Ser
CA1997992
NM_001256850.1:c.33613C>T