Canonical Allele Identifier: PA2830219162
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_597676.3:p.Ser14970Asn
CA16610376
NM_133432.3:c.44909G>A