Canonical Allele Identifier: PA2573193570
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1479779
ClinVar RCV Id: RCV001976919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34807Ser
CA349411769
NM_001267550.2:c.104421A>T
CA349411770
NM_001267550.2:c.104421A>C