Canonical Allele Identifier: PA103060
Gene: HAL HGNC NCBI

Linked Data

ClinVar Variation Id: 1691
ClinVar RCV Id: RCV000001759
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002099.1:p.Pro259Leu
CA115145
NM_002108.4:c.776C>T
CA1139532293
NM_002108.4:c.776_777delinsTG