Canonical Allele Identifier: PA2830237897
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332752
ClinVar RCV Id: RCV000269657 RCV000305320 RCV000308645 RCV000365690 RCV000406029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly19070Arg
CA10611610
NM_133437.4:c.57208G>A
CA349564215
NM_133437.4:c.57208G>C