Canonical Allele Identifier: PA311281
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro34061Leu
CA311280
NM_001256850.1:c.102182C>T