Canonical Allele Identifier: PA334131
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188133
ClinVar RCV Id: RCV000168008 RCV000236761 RCV000568153 RCV000662371 RCV001553594 RCV003995602
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu357Ala
CA017027
NM_000251.3:c.1070A>C