Canonical Allele Identifier: PA915983929
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134846
ClinVar RCV Id: RCV000121566 RCV000230947 RCV000409685 RCV000571485 RCV000587188 RCV002477316 RCV003483487 RCV003997350
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn8His
CA020232
NM_001258281.1:c.22A>C