Canonical Allele Identifier: PA2826428486
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2939853
ClinVar RCV Id: RCV003795019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33203Phe
CA1985409
NM_001256850.1:c.99608C>T