Canonical Allele Identifier: PA645410754
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264208
ClinVar RCV Id: RCV000247192 RCV000526468 RCV000828869 RCV001798754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro22740Ser
CA10587485
NM_001267550.2:c.68218C>T