Allele Registry

Canonical Allele Identifier: PA916011332

Gene: MSH6 HGNC NCBI

ClinVar Allele:

214603

ClinVar RCV:

RCV000202089

RCV000491378

RCV000501351

RCV001039124

RCV001353871

ClinVar Variation:

218057

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Asp928His	CA279731 NM_001281492.2:c.2782G>C