Canonical Allele Identifier: PA238213
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ser3945Leu
CA238211
NM_133379.5:c.11834C>T