Canonical Allele Identifier: PA104577
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16783
ClinVar RCV Id: RCV000018272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Ser541Arg
CA257626
NM_000400.4:c.1621A>C
CA406365310
NM_000400.4:c.1623C>G
CA406365311
NM_000400.4:c.1623C>A