Canonical Allele Identifier: PA2825113243
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073125
ClinVar RCV Id: RCV004015139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1678Lys
CA389037097
NM_000257.4:c.5034C>A
CA389037098
NM_000257.4:c.5034C>G