Canonical Allele Identifier: PA287454
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127646
ClinVar RCV Id: RCV000115530 RCV000199902 RCV000217044 RCV000411543 RCV001175574 RCV003997279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu135Phe
CA021136
NM_000251.3:c.403C>T