Canonical Allele Identifier: PA238321
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192093
ClinVar RCV Id: RCV000172486 RCV001129977 RCV001129978 RCV001129979 RCV001129980 RCV001129981 RCV002509280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala835Asp
CA238319
NM_001267550.2:c.2504C>A