Canonical Allele Identifier: PA916012088
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410535
ClinVar RCV Id: RCV000457877 RCV000490961 RCV002496783 RCV003148746 RCV003463944 RCV004001861
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His901Asn
CA16610976
NM_001281494.2:c.2701C>A