Canonical Allele Identifier: PA311308
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203120
ClinVar RCV Id: RCV000347920 RCV002345661 RCV000725471 RCV001084704 RCV001262304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Met1279Leu
CA311304
NM_133379.5:c.3835A>T
CA349477727
NM_133379.5:c.3835A>C