Canonical Allele Identifier: PA2825112194
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2704375
ClinVar RCV Id: RCV003586696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1065Asn
CA389045243
NM_000257.4:c.3194G>A