Canonical Allele Identifier: PA334092
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188119
ClinVar RCV Id: RCV000167977 RCV000223301 RCV000240465 RCV003454423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly164Glu
CA021218
NM_000251.3:c.491G>A