Canonical Allele Identifier: PA1139675118
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 924864
ClinVar RCV Id: RCV001186476 RCV001267836 RCV002339472 RCV001862934 RCV002491549 RCV003117820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1632Thr
CA044125
NM_000257.4:c.4894G>A