Canonical Allele Identifier: PA238286
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn1755Ser
CA238284
NM_001267550.2:c.5264A>G