Allele Registry

Canonical Allele Identifier: PA331807

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000114751

RCV000223291

RCV001216258

RCV003453034

ClinVar Variation:

126892

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ala1055Pro	CA011702 NM_000179.3:c.3163G>C