Canonical Allele Identifier: PA2826428985
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1469597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33711Pro
CA60953469
NM_001256850.1:c.101131T>C