Canonical Allele Identifier: PA095087
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90514
ClinVar RCV Id: RCV000076009 RCV000217955 RCV000508278 RCV000694503 RCV003452797
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro349Leu
CA016990
NM_000251.3:c.1046C>T