Canonical Allele Identifier: PA2830197836
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_596869.4:p.Ser19121Arg
CA349435478
NM_133378.4:c.57363C>G
CA349435480
NM_133378.4:c.57363C>A
CA349435491
NM_133378.4:c.57361A>C