Canonical Allele Identifier: PA2826464957
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 419432
ClinVar RCV Id: RCV000479030 RCV000688258 RCV001013864 RCV002230906 RCV003463995 RCV004002300
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr590Ser
CA16617598
NM_001258281.1:c.1769A>C