Canonical Allele Identifier: PA1139672272
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 915671
ClinVar RCV Id: RCV001170741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His401Gln
CA389051127
NM_000257.4:c.1203C>G
CA389051128
NM_000257.4:c.1203C>A