Canonical Allele Identifier: PA2826426269
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile30368Arg
CA1986834
NM_001256850.1:c.91103T>G