Canonical Allele Identifier: PA238301
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1206Ser
CA238299
NM_001267550.2:c.3616G>T