Canonical Allele Identifier: PA331392
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90798
ClinVar RCV Id: RCV000662761 RCV000708715 RCV001703978 RCV001218170 RCV003997154 RCV003317078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln61Pro
CA019414
NM_000251.3:c.182A>C