Allele Registry

Canonical Allele Identifier: PA2826463916

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000115497

RCV000206195

RCV000574856

RCV000663163

RCV001193851

RCV003997268

ClinVar Variation:

127628

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln336Lys	CA017489 NM_001258281.1:c.1006C>A