Canonical Allele Identifier: PA916066047
Gene: TTN HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser7451Ile
CA60987642
NM_133437.4:c.22352G>T