Canonical Allele Identifier: PA311753
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser4311Phe
CA311752
NM_001256850.1:c.12932C>T