Canonical Allele Identifier: PA190765
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185008
ClinVar RCV Id: RCV000164360 RCV000230583 RCV000485808 RCV000657018 RCV000662903 RCV003150015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala168Gly
CA015744
NM_000179.3:c.503C>G