Canonical Allele Identifier: PA2826429092
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1004601
ClinVar RCV Id: RCV001301330 RCV003135931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33822Arg
CA349405587
NM_001256850.1:c.101464G>A
CA349405590
NM_001256850.1:c.101464G>C