Canonical Allele Identifier: PA2826426667
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys31008Asn
CA1986463
NM_001256850.1:c.93024G>C
CA349435831
NM_001256850.1:c.93024G>T