Canonical Allele Identifier: PA645385035
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428382
ClinVar RCV Id: RCV000491517 RCV000797850 RCV000759147 RCV003464057 RCV004003460 RCV003316642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Phe1323Ser
CA46719891
NM_000179.3:c.3968T>C