Canonical Allele Identifier: PA310660
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn25612Ser
CA310659
NM_001256850.1:c.76835A>G