Canonical Allele Identifier: PA2579919650
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe650Leu
CA46700548
NM_000251.3:c.1948T>C
CA346728755
NM_000251.3:c.1950T>A
CA346728757
NM_000251.3:c.1950T>G