Canonical Allele Identifier: PA2828128881
Gene: MCPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350408
ClinVar RCV Id: RCV002039720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350908.1:p.Thr468Ser
CA4610543
NM_001363979.1:c.1403C>G
CA370221570
NM_001363979.1:c.1402A>T