Canonical Allele Identifier: PA2825113021
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2908745
ClinVar RCV Id: RCV003749048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1566Ser
CA257810700
NM_000257.4:c.4697A>G