Canonical Allele Identifier: PA1139673354
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 949541
ClinVar RCV Id: RCV001221015 RCV002393532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg507Ser
CA346746390
NM_000179.3:c.1521A>C
CA346746393
NM_000179.3:c.1521A>T