Canonical Allele Identifier: PA309042
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202308
ClinVar RCV Id: RCV000184147 RCV000554253 RCV001170834 RCV003137708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys16800Asn
CA309040
NM_001267550.2:c.50400A>T
CA349596373
NM_001267550.2:c.50400A>C