Canonical Allele Identifier: PA645474989
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232107
ClinVar RCV Id: RCV000213193 RCV000477485 RCV000791407 RCV000985799 RCV003469050 RCV004532791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr656Cys
CA032208
NM_000251.3:c.1967A>G