Canonical Allele Identifier: PA2826635632
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89240
ClinVar RCV Id: RCV000164083 RCV000223471 RCV000553788 RCV000781574 RCV003460668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser375Thr
CA009576
NM_001281494.2:c.1124G>C