Canonical Allele Identifier: PA285787
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96323
ClinVar RCV Id: RCV000259070 RCV000465659 RCV000723663 RCV002371932
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp31301Glu
CA285784
NM_001256850.1:c.93903C>G
CA349431556
NM_001256850.1:c.93903C>A