Canonical Allele Identifier: PA645409969
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229442
ClinVar RCV Id: RCV000214620 RCV002494575 RCV003327384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala16153Ser
CA10576523
NM_001267550.2:c.48457G>T