Canonical Allele Identifier: PA2830200153
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332761
ClinVar RCV Id: RCV000261667 RCV000315436 RCV000319078 RCV000354170 RCV000368850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly24607Ser
CA1989198
NM_133378.4:c.73819G>A