Canonical Allele Identifier: PA312008
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203313
ClinVar RCV Id: RCV000185409 RCV000275340 RCV000363577 RCV000304195 RCV000458691 RCV000329111 RCV000365247 RCV001798659 RCV003422080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala7157Thr
CA312007
NM_001256850.1:c.21469G>A