Canonical Allele Identifier: PA357406
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219569
ClinVar RCV Id: RCV000204403 RCV000519465 RCV000574858 RCV002243887 RCV003462366 RCV003997568
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.His388Asp
CA067228
NM_000179.3:c.1162C>G