Canonical Allele Identifier: PA2826635580
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2561260
ClinVar RCV Id: RCV003300982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser364Phe
CA068338
NM_001281494.2:c.1091C>T