Canonical Allele Identifier: PA312098
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203343
ClinVar RCV Id: RCV000185451 RCV000643774 RCV001293081 RCV003137761 RCV004539731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val8404Met
CA312097
NM_001256850.1:c.25210G>A