Canonical Allele Identifier: PA915956706
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 663735
ClinVar RCV Id: RCV000821674 RCV000995158 RCV003485650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn437Lys
CA389050888
NM_000257.4:c.1311C>A
CA389050889
NM_000257.4:c.1311C>G