Canonical Allele Identifier: PA2826414065
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn8007Lys
CA60970448
NM_001256850.1:c.24021C>A
CA349491342
NM_001256850.1:c.24021C>G