Canonical Allele Identifier: PA645411140
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332771
ClinVar RCV Id: RCV000288225 RCV000327544 RCV000333541 RCV000384466 RCV000385670 RCV000467844 RCV000516790 RCV000731987 RCV001798786 RCV002338920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu26302Asp
CA1989554
NM_001267550.2:c.78906A>C
CA349600653
NM_001267550.2:c.78906A>T