Canonical Allele Identifier: PA645412761
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282653
ClinVar RCV Id: RCV000277595 RCV000525933 RCV001170288 RCV001293057 RCV001293174 RCV001572757 RCV001840468 RCV001840469 RCV001840470 RCV001840471 RCV004543009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu34783Phe
CA1985436
NM_001267550.2:c.104347C>T