Allele Registry

Canonical Allele Identifier: PA2826587700

Gene: MSH6 HGNC NCBI

ClinVar Allele:

518483

ClinVar RCV:

RCV000630235

RCV000777010

ClinVar Variation:

525870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Leu1054Val	CA346761745 NM_001281494.2:c.3160T>G