Allele Registry

Canonical Allele Identifier: PA645378768

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000216536

RCV000476259

RCV000481509

RCV000659888

RCV000781606

RCV003462452

RCV003997874

ClinVar Variation:

230984

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg240Gln	CA073373 NM_000179.3:c.719G>A