Canonical Allele Identifier: PA310180
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202753
ClinVar RCV Id: RCV000184679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser18561Arg
CA310179
NM_001256850.1:c.55683C>G
CA349483610
NM_001256850.1:c.55683C>A
CA349483622
NM_001256850.1:c.55681A>C