Allele Registry

Canonical Allele Identifier: PA2826464466

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000204365

RCV000478447

RCV000570070

RCV001193995

RCV003150090

RCV003462360

RCV003997558

RCV004530216

ClinVar Variation:

219420

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr475Ile	CA348608 NM_001258281.1:c.1424C>T