Canonical Allele Identifier: PA179319
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166318
ClinVar RCV Id: RCV000152504 RCV000232506 RCV000621269 RCV001704105 RCV004544382
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met1557Ile
CA179317
NM_001256850.1:c.4671G>A
CA349462827
NM_001256850.1:c.4671G>C
CA349462829
NM_001256850.1:c.4671G>T