Canonical Allele Identifier: PA2825112454
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719081
ClinVar RCV Id: RCV002301841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1244Lys
CA389042829
NM_000257.4:c.3732C>G
CA389042830
NM_000257.4:c.3732C>A