Canonical Allele Identifier: PA132098
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43077
ClinVar RCV Id: RCV000035972 RCV001852733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn187Ser
CA016308
NM_000257.4:c.560A>G