Canonical Allele Identifier: PA658826704
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 560769
ClinVar RCV Id: RCV000679223 RCV001014567 RCV000812831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp715Glu
CA346751088
NM_000179.3:c.2145C>A
CA346751090
NM_000179.3:c.2145C>G