Allele Registry

Canonical Allele Identifier: PA658802415

Gene: MSH6 HGNC NCBI

ClinVar Allele:

518552

ClinVar RCV:

RCV000630191

RCV001018885

RCV004002795

ClinVar Variation:

525847

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile1054Val	CA070133 NM_000179.3:c.3160A>G