Canonical Allele Identifier: PA2826633964
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410463
ClinVar RCV Id: RCV000463911 RCV000485411 RCV000566983 RCV000662834 RCV003463934
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His1015Asp
CA072360
NM_001281493.2:c.3043C>G