Canonical Allele Identifier: PA2826587073
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410463
ClinVar RCV Id: RCV000463911 RCV000485411 RCV000566983 RCV000662834 RCV003463934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His1015Asp
CA072360
NM_001281494.2:c.3043C>G