Canonical Allele Identifier: PA2826426834
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser31274Gly
CA1986314
NM_001256850.1:c.93820A>G