Canonical Allele Identifier: PA2826465617
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821318
ClinVar RCV Id: RCV001015615 RCV003467625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val755Ala
CA346730523
NM_001258281.1:c.2264T>C