Canonical Allele Identifier: PA2826417254
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser14558Pro
CA237954
NM_001256850.1:c.43672T>C