Canonical Allele Identifier: PA2826414600
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502076
ClinVar RCV Id: RCV000598059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp9047Glu
CA1999659
NM_001256850.1:c.27141C>G
CA349440726
NM_001256850.1:c.27141C>A