Allele Registry

Canonical Allele Identifier: PA658680413

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000566160

RCV001055886

RCV003332204

RCV004001058

ClinVar Variation:

483814

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser330Pro	CA073692 NM_000179.3:c.988T>C