Allele Registry

Canonical Allele Identifier: PA2826635869

Gene: MSH6 HGNC NCBI

ClinVar Allele:

231555

ClinVar RCV:

RCV000223534

RCV000532996

RCV000564357

RCV000758666

ClinVar Variation:

234747

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg430Gln	CA068599 NM_001281494.2:c.1289G>A