Canonical Allele Identifier: PA180858
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177846
ClinVar RCV Id: RCV000154483 RCV000172890 RCV000208237 RCV000577993 RCV000578027 RCV000578112 RCV000464078 RCV000724585 RCV000769433 RCV002483337 RCV002345494 RCV003320110
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1763Thr
CA015861
NM_000257.4:c.5287G>A