Canonical Allele Identifier: PA645417494
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312894
ClinVar RCV Id: RCV000281905 RCV000297103 RCV000336900 RCV000404092 RCV001094164 RCV003320155 RCV003129830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1610Lys
CA10645050
NM_000257.4:c.4828G>A