Canonical Allele Identifier: PA2826426266
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1755953
ClinVar RCV Id: RCV002362242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu30366Asp
CA1986838
NM_001256850.1:c.91098A>C
CA349454817
NM_001256850.1:c.91098A>T