Canonical Allele Identifier: PA2829436491
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_003310.4:p.Ser12624Arg
CA349435478
NM_003319.4:c.37872C>G
CA349435480
NM_003319.4:c.37872C>A
CA349435491
NM_003319.4:c.37870A>C