Canonical Allele Identifier: PA658671732
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483679
ClinVar RCV Id: RCV000574683 RCV000810913
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu187Phe
CA346730909
NM_000251.3:c.559C>T