Canonical Allele Identifier: PA2830206711
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202343
ClinVar RCV Id: RCV000184185 RCV000643624 RCV000852929 RCV002390475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr2543Ser
CA309149
NM_133378.4:c.7628C>G
CA349679335
NM_133378.4:c.7627A>T