Canonical Allele Identifier: PA169068
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142663
ClinVar RCV Id: RCV000132010 RCV000234247 RCV000412120 RCV000484116 RCV000708888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1151Gly
CA012948
NM_000179.3:c.3452C>G