Canonical Allele Identifier: PA167661
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142169
ClinVar RCV Id: RCV000131137 RCV000464371 RCV000481281 RCV003447501 RCV003998086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His424Tyr
CA017712
NM_000251.3:c.1270C>T