Canonical Allele Identifier: PA2741847107
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3026501
ClinVar RCV Id: RCV003886894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser21689Arg
CA349435478
NM_001267550.2:c.65067C>G
CA349435480
NM_001267550.2:c.65067C>A
CA349435491
NM_001267550.2:c.65065A>C