Canonical Allele Identifier: PA2579923984
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795200
ClinVar RCV Id: RCV002431299
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys907Asn
CA346731782
NM_000251.3:c.2721G>C
CA346731784
NM_000251.3:c.2721G>T