Canonical Allele Identifier: PA310323
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202798
ClinVar RCV Id: RCV000643672 RCV001311238 RCV001798653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly20291Arg
CA310322
NM_001256850.1:c.60871G>A
CA349432636
NM_001256850.1:c.60871G>C