Canonical Allele Identifier: PA645410886
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404947
ClinVar RCV Id: RCV000464411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser23910Asn
CA16610376
NM_001267550.2:c.71729G>A