Canonical Allele Identifier: PA212685
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42822
ClinVar RCV Id: RCV000035698 RCV000223685 RCV000487437 RCV000491937 RCV000544985 RCV000587847 RCV001798093 RCV003320043 RCV004545737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg369Gln
CA010192
NM_000257.4:c.1106G>A