Canonical Allele Identifier: PA2580177307
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_001254479.2:p.Thr35341Ser
CA349407201
NM_001267550.2:c.106022C>G
CA349407203
NM_001267550.2:c.106021A>T