Canonical Allele Identifier: PA2826421646
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 501630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu22479Phe
CA1990511
NM_001256850.1:c.67435C>T