Canonical Allele Identifier: PA141235
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47513
ClinVar RCV Id: RCV000040782 RCV000172620 RCV000282263 RCV000295443 RCV000316301 RCV000352604 RCV000373589 RCV000457779 RCV002362644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly30541Arg
CA141232
NM_001267550.2:c.91621G>A
CA349499579
NM_001267550.2:c.91621G>C