Canonical Allele Identifier: PA916011723
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 520541
ClinVar RCV Id: RCV000622394 RCV003594011 RCV003278952 RCV003451475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His65Arg
CA346741910
NM_001281494.2:c.194A>G