Canonical Allele Identifier: PA2830238767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47473
ClinVar RCV Id: RCV000040742 RCV000270510 RCV000327903 RCV000362829 RCV000384731 RCV000334082 RCV000618175 RCV000475243 RCV000725444 RCV001798192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly20491Ser
CA141118
NM_133437.4:c.61471G>A