Allele Registry

Canonical Allele Identifier: PA2826633622

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000121589

RCV000160698

RCV000206271

RCV000411602

RCV000656902

RCV003460856

RCV003997354

ClinVar Variation:

134856

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Val951Ala	CA014193 NM_001281493.2:c.2852T>C