Canonical Allele Identifier: PA2826625518
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219569
ClinVar RCV Id: RCV000204403 RCV000519465 RCV000574858 RCV002243887 RCV003462366 RCV003997568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His258Asp
CA067228
NM_001281492.2:c.772C>G