Canonical Allele Identifier: PA2573165083
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1467571
ClinVar RCV Id: RCV001993441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn911Lys
CA389047233
NM_000257.4:c.2733C>G
CA389047234
NM_000257.4:c.2733C>A