Canonical Allele Identifier: PA357612
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220025
ClinVar RCV Id: RCV000205795 RCV000481152 RCV000657148 RCV001180058 RCV003997604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser271Cys
CA349912
NM_000251.3:c.812C>G