Canonical Allele Identifier: PA207950
Gene: MYH8 HGNC NCBI

Linked Data

ClinVar Variation Id: 211567
ClinVar RCV Id: RCV000194050 RCV000210686 RCV000953038 RCV000989748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002463.2:p.Arg1784Gly
CA207949
NM_002472.3:c.5350C>G