Canonical Allele Identifier: PA185204
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 179817
ClinVar RCV Id: RCV000156616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn224Thr
CA016618
NM_000257.4:c.671A>C