Allele Registry

Canonical Allele Identifier: PA2826636897

Gene: MSH6 HGNC NCBI

ClinVar Allele:

94796

ClinVar RCV:

RCV000218618

RCV000455514

RCV000629775

RCV002273954

RCV003460673

ClinVar Variation:

89322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg674His	CA011105 NM_001281494.2:c.2021G>A