Canonical Allele Identifier: PA645412139
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn31567Ser
CA10604814
NM_001267550.2:c.94700A>G