Canonical Allele Identifier: PA2826417469
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val14960Leu
CA1994514
NM_001256850.1:c.44878G>T
CA349600959
NM_001256850.1:c.44878G>C