Canonical Allele Identifier: PA2499230305
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1041888
ClinVar RCV Id: RCV001345762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln222His
CA389052297
NM_000257.4:c.666G>T
CA389052298
NM_000257.4:c.666G>C