Canonical Allele Identifier: PA2826426099
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132138
ClinVar RCV Id: RCV000119026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn30145Lys
CA358830
NM_001256850.1:c.90435C>G
CA349462615
NM_001256850.1:c.90435C>A