Canonical Allele Identifier: PA2826465988
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 479786
ClinVar RCV Id: RCV000572179 RCV000697646 RCV004000845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val849Ala
CA346731919
NM_001258281.1:c.2546T>C