Canonical Allele Identifier: PA2826464010
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142169
ClinVar RCV Id: RCV000131137 RCV000464371 RCV000481281 RCV003447501 RCV003998086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His358Tyr
CA017712
NM_001258281.1:c.1072C>T