Canonical Allele Identifier: PA2826464802
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489926
ClinVar RCV Id: RCV000579741 RCV000630172
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Pro552Leu
CA346728438
NM_001258281.1:c.1655C>T