Canonical Allele Identifier: PA2826636704
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127574
ClinVar RCV Id: RCV000115395 RCV000212671 RCV000206053 RCV000587183 RCV001253566 RCV003460815 RCV003997243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile625Thr
CA010911
NM_001281494.2:c.1874T>C