Canonical Allele Identifier: PA645411925
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 264301
ClinVar RCV Id: RCV000251890 RCV000642979 RCV000827153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys30053Asn
CA10587455
NM_001267550.2:c.90159A>C
CA349513405
NM_001267550.2:c.90159A>T