Allele Registry

Canonical Allele Identifier: PA095114

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000129083

RCV000236043

RCV000627734

RCV000656871

RCV000662483

RCV001354855

RCV002483125

RCV003997185

ClinVar Variation:

91267

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Thr33Pro	CA022692 NM_000251.3:c.97A>C