Canonical Allele Identifier: PA645380502
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428340
ClinVar RCV Id: RCV000491862 RCV000822280 RCV003464048 RCV004003456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser536Thr
CA346746995
NM_000179.3:c.1607G>C