Canonical Allele Identifier: PA1139673499
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 849092
ClinVar RCV Id: RCV001052979 RCV001181500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu903Asp
CA389047313
NM_000257.4:c.2709G>C
CA389047314
NM_000257.4:c.2709G>T