Canonical Allele Identifier: PA1139674623
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 923297
ClinVar RCV Id: RCV001183872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp713Glu
CA346751066
NM_000179.3:c.2139T>A
CA346751067
NM_000179.3:c.2139T>G