Canonical Allele Identifier: PA2573165095
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349456
ClinVar RCV Id: RCV002046951
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys635Asn
CA346728612
NM_000251.3:c.1905A>C
CA346728613
NM_000251.3:c.1905A>T