Canonical Allele Identifier: PA2826628419
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_001268421.1:p.Ala1021Gly
CA012948
NM_001281492.2:c.3062C>G