Canonical Allele Identifier: PA2825088243
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772977
ClinVar RCV Id: RCV002394633
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu484Asp
CA346745706
NM_000179.3:c.1452A>C
CA346745710
NM_000179.3:c.1452A>T