Canonical Allele Identifier: PA2830200183
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn24685Ser
CA310659
NM_133378.4:c.74054A>G