Canonical Allele Identifier: PA2826424728
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr27955Ser
CA237725
NM_001256850.1:c.83864C>G
CA349524843
NM_001256850.1:c.83863A>T