Canonical Allele Identifier: PA141621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47654
ClinVar RCV Id: RCV000040923 RCV000462618 RCV001293170 RCV001703916 RCV002390174 RCV003149664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34246His
CA141618
NM_001267550.2:c.102737G>A