Canonical Allele Identifier: PA916011650
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182618
ClinVar RCV Id: RCV000160663 RCV000198861 RCV000212644 RCV000662570 RCV001798553 RCV002271427 RCV003998491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly52Val
CA007928
NM_001281494.2:c.155G>T