Canonical Allele Identifier: PA2826410907
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn1755Ser
CA238284
NM_001256850.1:c.5264A>G