Canonical Allele Identifier: PA337857
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216302
ClinVar RCV Id: RCV000198361 RCV000213164 RCV000411644 RCV000781573 RCV001357273 RCV001580468 RCV003996996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys632Glu
CA068250
NM_000179.3:c.1894A>G