Canonical Allele Identifier: PA2826423876
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr26509His
CA140988
NM_001256850.1:c.79525T>C