Canonical Allele Identifier: PA141126
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe27754Leu
CA141123
NM_001256850.1:c.83260T>C
CA349530998
NM_001256850.1:c.83262C>G
CA349531001
NM_001256850.1:c.83262C>A