Canonical Allele Identifier: PA238158
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192036
ClinVar RCV Id: RCV000172417 RCV000217501 RCV000544990 RCV000620036 RCV003486720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser4274Asn
CA238157
NM_001267550.2:c.12821G>A