Canonical Allele Identifier: PA2826428972
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2016721
ClinVar RCV Id: RCV002851719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr33700Ser
CA349407201
NM_001256850.1:c.101099C>G
CA349407203
NM_001256850.1:c.101098A>T